- Original Article
- Respiratory syncytial virus-associated seizures in Korean children, 2011–2016
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Teahyen Cha, Young Jin Choi, Jae-Won Oh, Chang-Ryul Kim, Dong Woo Park, In Joon Seol, Jin-Hwa Moon
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Clin Exp Pediatr. 2019;62(4):131-137. Published online October 23, 2018
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Purpose: Respiratory syncytial virus (RSV) infection can cause various neurological complications. This study aimed to investigate the RSV-associated neurologic manifestations that present with seizures.
Methods: We retrospectively reviewed the medical records of patients aged less than 15 years with laboratory-confirmed RSV infections and seizures between January 2011 and December 2016 in a regional hospital in South Korea.
Results: During this period, 1,193... |
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- Case Report
- Neurology
- A new mosaic der(18)t(1;18)(q32.1;q21.3) with developmental delay and facial dysmorphism
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Young-Jin Choi, Eunsim Shin, Tae Sik Jo, Jin-Hwa Moon, Se-Min Lee, Joo-Hwa Kim, Jae-Won Oh, Chang-Ryul Kim, In Joon Seol
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Clin Exp Pediatr. 2016;59(2):91-95. Published online February 29, 2016
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We report the case of a 22-month-old boy with a new mosaic partial unbalanced translocation of 1q and 18q. The patient was referred to our Pediatric Department for developmental delay. He showed mild facial dysmorphism, physical growth retardation, a hearing disability, and had a history of patent ductus arteriosus. White matter abnormality on brain magnetic resonance images was also noted.... |
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- Original Article
- Medicolegal Problems in Pediatric Area
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Soo Jeong Kwon, Ji Young Jang, Nam Su Kim, Myung Kul Yum, In Joon Seol, Ku Won Jung
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Clin Exp Pediatr. 2005;48(8):813-819. Published online August 15, 2005
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Purpose : Medicolegal problems start when the patient asserts the mistake of doctor and doctor does not accept it. The purpose of this study is to assess the actual condition of medicolegal problems and to provide solutions of medicolegal problems in the pediatric field.
Methods : There is not official statistical data about medicolegal problems in our country. We gathered... |
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- Case Report
- A Case of Sandifer Syndrome
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Mira Lee, Soo Hyun Kim, Yong Joo Kim, In Joon Seol
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Clin Exp Pediatr. 2003;46(10):1036-1039. Published online October 15, 2003
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Sandifer syndrome is a rare manifestation of gastroesophageal reflux in children, occurring in association with abnormal movement of the head and neck and recurrent episodes of seizure after feeding. This syndrome may be misdiagnosed as infantile seizure and musculoskeletal disorder and may be associated with failure to thrive, anemia, aspiration pneumonia, and esophagitis. In this paper, Sandifer syndrome in a... |
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- Original Article
- The Usefulness of Emergency Brain Computerized
Tomography in Children with First Seizures
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Hyun Kyung Park, In Joon Seol
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Clin Exp Pediatr. 2001;44(5):562-568. Published online May 15, 2001
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Purpose : This study was performed to discover whether emergency brain computerized tomography(CT) is useful for the diagnosis and management of patients with first seizure.
Methods : We studied retrostpectively all children(under 15-year-old) without a history of neurologic illness who visited Hanyang University Hospital and took a brain CT because of a first seizure attack between January 1996 and June 1999.... |
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- Case Report
- A Case of Atypical Benign Partial Childhood Epilepsy
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Hae Jung Park, In Joon Seol
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Clin Exp Pediatr. 2001;44(2):211-215. Published online February 15, 2001
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We report a case of atypical benign partial childhood epilepsy in a 11 years old male child whose case has been followed up for 6 years. His first symptom was focal seizure of the left side of his face during a drowsy state, followed by focal seizures of left fingers and legs. At that time he had been on phenobarbital... |
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- Original Article
- A Study on the Clinical Significance of Periodic Lateralized Epileptiform Discharges and Relation to Brain Imaging Study in Children
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Jong Hwa Lee, Eun Young Park, Nam Su Kim, In Joon Seol
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Clin Exp Pediatr. 2000;43(3):380-385. Published online March 15, 2000
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Purpose : Periodic lateralized epileptiform discharges(PLEDs), initially described by Chatrian et al in 1964, are an EEG phenomenon characterized by lateralized or focal spike-and-wave complexes with moderate to high voltage which occur in a periodic or semiperiodic pattern. This study was performed to assess the clinical significance of PLEDs and its relation to an imaging study of the brain.
Methods :... |
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- Study on Serum Level of Phenobarbital after Intravenous Administration of Loading Dose
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Eun Young Park, In Joon Seol
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Clin Exp Pediatr. 1998;41(10):1403-1410. Published online October 15, 1998
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Purpose : To learn the changes of phenobarbital serum level after intravenous administration of loading dose and to determine the optimal time of maintenance therapy to support therapeutic concentration.
Methods : A total of 24 patients, who were admitted to the pediatric ward for treatment of ongoing and recurrent seizure, were enrolled in this study from November, 1994 to August,... |
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- A Study on the Serum Level of Phenytoin after Intravenous Administration of Loading Dose
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In Joon Seol, Young Iee Yu
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Clin Exp Pediatr. 1997;40(10):1435-1442. Published online October 15, 1997
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Purpose : Phenytoin is effectively and widely used drug for the treatment of status
epilepticus and patient with ongoing seizure by intravenous infusion. It is generally
recommended to maintain serum concentration above 10μg/ml for the sustained effective
anticonvulsant effect. This study was designed to know the optimal time to begin oral
maintenance therapy after initial intravenous infusion.
Methods : Total 17 patients with status epilepticus... |
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- Case Report
- A Case of Cerebral Infarction Associated with Mycoplasma pneumoniae Infection
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Young Jae Koh, Dong Jun Kim, In Joon Seol, Ha Baik Lee, Ki Woong Hong
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Clin Exp Pediatr. 1996;39(1):115-119. Published online January 15, 1996
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Mycoplasma pneumoniae has been shown to be of etiologic importance in cases of upper-and lower-respiratory tract infections, especially in children and young adults. It may cause a variety of extrapulmonary manifestations in multiple organ systems, most commonly the central nervous system. The extrapulmonary syndromes include meningitis, cerebral infarction, acute transverse myelitis, psychosis, cerebellar ataxia, Guillain-Barré syndrome and Reye syndrome. Cerebral... |
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- Case Report
- A Case of Defecation-induced Epilepsy
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Dong Nam Kim, In Seung Park, In Joon Seol
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Clin Exp Pediatr. 1995;38(1):138-140. Published online January 15, 1995
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Defecation induced epilepsy is a very rare form of reflex epilepsy, which has not been reported yet in Korea. We experienced a case of defecation-induced epilepsy in a 10 month old boy who has been showing seizure with every defecation since 5 months of his age. Diagnosis was made by clinical history and appearance of clinical seizure with epileptiform activities... |
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- Original Article
- Occult Mediastinal Ganglioneuroblastoma Presenting with Myoclonic Encephalopathy as Paraneoplastic Syndrome
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Hahng Lee, Dong Ki Han, Jae Won Oh, In Joon Seol, Eun Kyung Hong, Seok Chol Jeon
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Clin Exp Pediatr. 1994;37(5):695-700. Published online May 15, 1994
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Ganglioneruroblastoma and neuroblastoma are among commonest types of childhood malignancy and a number of unique paraneoplastic syndromes have been associated with both localized and disseminated neuroblastoma. The coincidence of neuroblastoma and myoclonic encephalopathy or other paraneoplastic syndromes occurs relatively rare, and therefore, failure to recognize this association could result in delays in both diagnosis and treatment, and the result... |
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- Case Report
- A Case of Rotor Syndrome
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Jin Nyoung Park, In Joon Seol
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Clin Exp Pediatr. 1994;37(3):410-415. Published online March 15, 1994
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We experienced a case of Rotor syndrome in an 8 year 6 month old boy who presented with icteric sclera and icteric skin on whole body. His clinical and laboratory characteristics were as follows;
1) Jaundice appeared from several months ago before admission without any clinical disturbance.
2) Direct bilirubin was more increased than indirect bilirubin.
3) Plasma indocyanine green (ICG) kinetics test... |
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- Original Article
- A Study on Prognostic Factors in Children with Encephalopathy
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Jin Nyoung Park, In Joon Seol
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Clin Exp Pediatr. 1994;37(12):1738-1745. Published online December 15, 1994
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To elucidate the clinical characteristics-especially its clinical pattern and outcome of chidren with encephalopathy, we carried out a retrospective review on medical records of 45 patients who were intially diagnosed as encephalopathy except mumps meningitis, Reye's syndome and neonatal hypoxic ischemic encephalopathy at the Department of pediatrics, Hanyang University children's hospital from January 1986 to February 1994.
The results were summerized... |
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- The Study on the Clinical Significance of the Finger Extension Reflex in Early Infancy
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Seong Yeob Moon, In Joon Seol
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Clin Exp Pediatr. 1994;37(10):1350-1356. Published online October 15, 1994
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The finger extension reflex was performed to the 419 normal infants without CNS abnormalities that visited to the well baby clinic and out-patient department, and so to the patients with CNS abnormalities on the brain sonography and brain CT under the age of 2 months from May 1992 to September 1993 in the department of pediatrics, Hanyang university hospital.
The results... |
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- Clincal Observation on Guillain-Barré Syndrome in Children
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In Cheol Park, In Seung Park, Jeh Hoon Shin, In Joon Seol, Ha Baik Lee
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Clin Exp Pediatr. 1993;36(5):634-642. Published online May 15, 1993
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Clinical observation was performed on 23 children with Guillain-Barré syndrome which were hospitalized at the Pediatric ward of Han Yang University Hospital, from July 1975 through May 1991.
The results were as follows:
1)The ratio of male patient to female was 2.8:1 and 47.8% of total GBS patients were between the ages 1to 5 years.
2)The highest seasonal incidence of GBS was seen... |
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- Study on the Frequency of Right Bundle Branch Block After Surgical Closure of Ventricular Septal Defect
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Ho Joon Im, Jin Nyoung Park, Nam Su Kim, Jeh Hoon Shin, In Joon Seol, Soo Ji Moon
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Clin Exp Pediatr. 1993;36(1):88-93. Published online January 15, 1993
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The purpose of this study is to evaluate the ventricular conduction abnormalities, especially RNNN, observed electrocardiographically after sugical closure of VSD.
The present study population consists of 92 patients with VSD who were surgically corrected at the Hanyang University Hospital during 6 years period from Jan. 1985 to Dec. 1990. We reviewed their clinical records including surgical notes and EKG findings... |
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- Case Report
- A Case of Neuronal Ceroid-Lipofuscinosis with characterstic photic evoked spikes in EEG
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Joo Hyun Han, Jae Won Oh, Jae Hoon Shin, In Joon Seol, Young Hyae Koh, Moon Hyang Park
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Clin Exp Pediatr. 1992;35(2):252-256. Published online February 15, 1992
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We experienced a case of neuronal ceroid lipofuscinosis in a 1 year old female child. Her chief complaints on admission were retarded growth and development, recurrent seizures and hypotonia.
Electroencephalographic examination showed very characteristic photic responses, so called, photic evoked spikes which are synchronous with the flashes at 5 flashes per second. Final diagnosis was made with electron microscopic examination of... |
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- A Case of Video Game Epilepsy
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Jin Nyoung Park, Ho Joon Im, Sung Lae Park, Jeh Hoon Shin, In Joon Seol, Soo Ji Moon
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Clin Exp Pediatr. 1992;35(12):1756-1761. Published online December 15, 1992
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Video game epilepsy is a photic induced sensory evoked seizure, and the seizure occurs only following a specific program of video game.
We experienced a case of video game epilepsy in a 12 year old boy who presented with seizure during video game, and showed photoconvulsive response on photic stimulated EEG. |
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- A Case of Salmonella Group C Meningitis
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Dae Chul Kim, Ju Hyun Han, So Young Lee, Jeh Hoon Shin, In Joon Seol
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Clin Exp Pediatr. 1992;35(10):1449-1453. Published online October 15, 1992
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We experienced a case of salmonella group C meningits in a 3 month old male. His initial chief complaints at the admission were high fever, lethargy, irregular respiration and arrythmias.
Diagnosis was confirmed by lumbar puncture, blood culture and CSF culture. Ceftriaxone was used and recovered with some sequelae such as irritability, generalized spasticity and mild regression of psychomotor development. |
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- Original Article
- Clinical Study of Group B Streptococcal Infection in Infants Less Than Two Months of Age
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Hee Jeong Ahn, Ji Yeon Lim, Sung Hee Oh, In Joon Seol, Soo Jee Moon, Hahng Lee
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Clin Exp Pediatr. 1992;35(1):17-25. Published online January 15, 1992
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Since 1970, the group B streptococcus has become significant cause of neonatal septicemia and/or meningitis, in recent years the group B streptococcus and E.coli are most common etiologic agent of septicemia and/or meningitis in infants less than two months of age. We have analized 8 cases of group B streptococcal infection who admitted to the department of Pediatrics, Hanyang University... |
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- A clinical study on twin.
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Ho Joon Im, Sang Yoon Ahn, In Joon Seol, Soo Jee Moon, Hahng Lee
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Clin Exp Pediatr. 1991;34(5):621-628. Published online May 31, 1991
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Among the total of 17,991 newborns delivered at Hanyang University Howpital from January 1980
to December 1989, a clinical study was performed on 277 twin pregnancies.
The results of the study were as follows:
1) The incidence of twins was 1:64.9.
2) The average male-female sex ratio of twins was 1:1.1, total same sex pairs rate was 79.4%
(male-male & female-female) and different sex rate was 20.6%.
3) The... |
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- A case of report fiber syndrome.
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So Young Lee, Sun Yang Hong, Jae Hoon Shin, In Joon Seol
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Clin Exp Pediatr. 1991;34(1):115-119. Published online January 31, 1991
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This is a report of 10 years old boy whose complete total ophthalmoplegia, ataxia and areflexia
(Fisher syndrome) were the outstanding clinical features. |
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- A case of interstitial pulmonary fibrosis.
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Hak Won Kim, Ho Joon Im, In Joon Seol, Ha Baik Lee, Hahng Lee, Seok Chol Jeon, Moon Hyang Park
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Clin Exp Pediatr. 1991;34(1):107-114. Published online January 31, 1991
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Interstitial pulmonary fibrosis is a rare, diffuse lug disease which has a tendency to destroy the lung
architectures by consequent healing with progressively severe fibrosis.
We report with a brief review of literature, one case of a 7-year old female with the typical pictures
of interstitial pulmonary fibrosis, histologically on open lung biopsy, and clinically presenting with
chronic respiratory difficulty but without definite symptoms... |
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- A clinical and Statistical study of Meconium Stained Baby: A Two Year Prospective Study.
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Joo Hyun Ham, Sang Yoon Ahn, In Joon Seol, Soo Jee Moon, Hahng Lee
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Clin Exp Pediatr. 1990;33(9):1173-1179. Published online September 30, 1990
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Among the total of 2,483 Newborns delivered at Hanyang University Hospital from January 1987
to December 1988, a clinical study was performed of meconium stained baby.
The results are summerized as follows:
1) The incidence of meconium staining was 13.4% (333 cases) in total 2,483 newborns.
2) In the groups that the birth weight is 2501 ~ 4000 gm and up to 4001 gm, the incidence... |
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- A Case of Malignant Ependymoma.
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Ja Wook Koo, Sun Ho Lee, In Joon Seol, Hahng Lee
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Clin Exp Pediatr. 1989;32(1):130-136. Published online January 31, 1989
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Intracranial tumors presenting in the first year of life are uncommon. Brain tumors in infancy are
predominantly supratentorial, whereas in older children the majority are infratentorial. Malignant
ependymoma is a rare type of primitive ependymal tumor with clinically high malignancy.
We experienced a malignant ependymoma in a 5 month old girl who had progressive enlargement
of head circumference with vomiting. Brain computed tomography revealed... |
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- A Case of Paroxysmal Kinesigenic Choreoathetosis.
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Jeong Kook Lee, In Joon Seol
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Clin Exp Pediatr. 1989;32(1):116-120. Published online January 31, 1989
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Paroxysmal choreoathetosis is a rare, involuntary movement disorder, wich occur spontaneously or
may be induced by movement, startle or anxiety.
The attacks are tonic, dystonic or choreoathetotic without loss of consciousness, urinary inconti-
nence, or amnesia.
The atacks begin most often in school aged years and the course is nonprogressive.
The response to anticonvulsant therapy is usually excellent, We report a case of paroxysmal
kinesigenic choreoathetosis... |
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- A Case of Mollaret Meningitis.
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Yong Joo Kim, Soon Sup Jang, In Joon Seol
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Clin Exp Pediatr. 1988;31(9):1193-1196. Published online September 30, 1988
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Mollaret meningitis is a benign recurrent aseptic meningitis. We experienced a case of Mollaret
meningitis in a 5 years old male child. He has had 4 times of recurrent aseptic meningitis after
antecedent viral infection which showed meningeal irritation signs, weakness of lower extremities
and urination difficulties.
We present a case of Mollaret meningitis with brief review of related literatures. |
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- Lateral Ventricular Indices in tuberculous Meningitis.
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Ja Wook Koo, Hang Bo Cho, In Joon Seol, soo Jee Moon, Hahng Lee, Keun Soo Lee
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Clin Exp Pediatr. 1988;31(8):984-991. Published online August 31, 1988
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Computed tomography is a very valuable method by which the pathogenic evolution of tuberculous
meningitis may be followed, thereby facillitating its differential diagnosis and controlling the effi-
ciency of therapy, and assessing the degree of hydrocephalus.
Fifteen cases of clinically proven intracranial tuberculosis were studied by lateral ventricular
indices of brain computed tomography in our hospital during last 3 years.
The results were as follows:
1)... |
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- Clinical Characteristics and Pathogenesis of Typhlitis in Childhood Non-Lymphocytic Leukemia-Considerations on Clinical Mangement with Report of Two Cases and Literature Review.
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Do Hyun Kim, Sung Oh Kim, Soo Yup Lee, In Joon Seol, Hahng Lee, Chong Moo Park, Poong Man Jung, Seok Chol Jeon, Young Hyeh Ko, Jung Dal Lee
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Clin Exp Pediatr. 1988;31(5):607-620. Published online May 31, 1988
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The treatment of acute leukemia in childhood has been increasingly successful due to progression
of chemotherapeutics and other supportive care. Improved survival rates in acute childhood leukemia
have been associated with an increasing number of complications in the gastrointestinal tract.
Typhlitis also known as ileocecal syndrome is a necrotizing inflammation of the cecum in leukemic
patients on chemotherapy in the terminal stage of the... |
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- A Statistical Study of the Children with Congenital Heart Diseases confirmed by Cardiac Catheterization and Cineangiography.
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Jeong Kook Lee, Hang Bo Cho, Soo Yup Lee, In Joon Seol, Kyoo Whan Rhee, Chong Moo Park
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Clin Exp Pediatr. 1988;31(2):153-160. Published online February 28, 1988
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In a total of 537 cases the diagnosis of congenital heart disease and the types of cardiac anomalies
were confirmed by cardiac catheterization and cineangiography during the period of 56 months from
September 1982 to April 1987 at Hanyang University Hospital and these patients studied were
analyzed statistically for the frequency of each individual type of cardiac anomalies.
The summary of the findings are... |
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- Cineaortography by Countercurrent Injection via the Radial Artery in Neonates and Infants.
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Do Hyun Kim, Hong Kun Kim, In Joon Seol, Kyoo Hwan Lee, Goo Hwan Je
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Clin Exp Pediatr. 1987;30(7):716-721. Published online July 31, 1987
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Cineaortography by countercurrent injection via the radial artery was performed for the diagnosis
of aortic arch anomalies in four infants with congenital heart anomalies. A patent ductus arteriosus,
a hypoplastic pulmonary arteries and a normal aortic arch were demonstrated respectively by this
method. The complete obstruction at the site of shunt operation for tricuspid atresia type lb was
confirmed in the post operative period.... |
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- Case Report
- A Case of Holoprosencephaly.
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Byung Chun Suh, Soon Sup Jang, In Joon Seol, Soo Jee Moon, Chong Moo Park, Seok Chol Jeon
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Clin Exp Pediatr. 1987;30(6):695-700. Published online June 30, 1987
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We experienced a case of holoprosencephaly with extracranial abnormalities, including orbital
hypotelorism, median cleft lip without philtrum, flat nasal bridge, flat face, and microcephaly and
with a karyotype, 46 XX, 22p+.
The diagnosis was confirmed by brain CT scan & brain ultrasonography, and the findings were
compatible with an alobar type of holoprosencephaly. The patients died at 26 days of age.
A brief review of... |
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- Original Article
- A Clinical and Laboratory Study on Infection in Childhood Leukemia.
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Jung Hee Lee, Kwang Hyun Kim, In Joon Seol, Heung Jae Lee, Hahng Lee, Chong Moo Park
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Clin Exp Pediatr. 1986;29(7):699-709. Published online July 31, 1986
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Acute Leukemia is the most common among malignant disease in childhood, and the loss of normal hematopoiesis by proliferation of leukemic cells and the chemotherapy result in immunosuppression and the reduction of red blood cells, normal white blood cells and platelets. The children with acute leukemia may succumb to the disease due to infections, hemorrhage, other complications, or the progression... |
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- Case Report
- A case of Sacrococcygeal Teratoma.
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Seung Jae Yang, Kwang Nam Kim, In Joon Seol, Soo Jee Moon, Keun Soo Lee
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Clin Exp Pediatr. 1986;29(5):564-569. Published online May 31, 1986
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We exprienced a case of sacrococcygeal teratoma in newborn girl with massive intraabdominalfextensioii and small caudal mass, which is relative rare.
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- Original Article
- A Study on Four Serum Enzymes in Acute Leukemia in Children.
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In Joon Seol, Seung Jae Yang, Kyoo Hwan Rhee, Hahng Lee, Chong Moo Park, Jae Kyung Koh
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Clin Exp Pediatr. 1986;29(2):130-142. Published online February 28, 1986
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In order to find out whether some of serum enzyme levels could be used as markers for acute leukemia in children, activities of amylase, alkaline phosphatase, 5 -nucleotidase and ribonuclease (RNase) and positive rates of these enzymes as markers for acute leukemia in children were determined in serum of patients with acute lymphocytic leukemia (ALL) and acute non-lymphocytic leukemia(ANLL).
Since the... |
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- Case Report
- A Case of Agenesis of the Corpus Callosum.
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Jung Hee Lee, Seong Ryong Hyun, In Joon Seol, Ha Baik Lee, Keun Soo Lee
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Clin Exp Pediatr. 1985;28(8):836-840. Published online August 31, 1985
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Agenesis of the corpus callosum is a relatively common malformation that may occur in isolation or in combination with other cerebral malformation. We experienced a case of agenesis of the corpus callosum in a 5/12 year old boy who showed developmental retardation. Cerebral brian CT and sonography demonstrated a typical picture of agenesis of the corpus callosum without any further... |
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- Original Article
- Pre-and Postoperative Evaluation of Patent Ductus Arteriosus in Children.
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In Hee Park, Jung Hee Lee, In Joon Seol, Heung Jae Lee
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Clin Exp Pediatr. 1985;28(7):683-694. Published online July 31, 1985
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During a period of IOV12 years, from April, 1974 to July, 1984, 92 cases under 15 years of age with isolated patent ductus arteriosus were observed and evaluated pre- and postoperatively at pediatric department, Hanyang University Hospital, and those were confirmed by cardiac catheterization and/or surgery.
The summary of observation made is as follows: 1)The sex ratio of male to female... |
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- Case Report
- A Case of Hutchinson-Gilford Progeria Syndrome.
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Seon Ock Khang, Jung Hee Lee, In Joon Seol, Gwi Jong Choi, Keun Soo Lee
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Clin Exp Pediatr. 1985;28(4):405-410. Published online April 30, 1985
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Hutchinson-Gilford progeria syndrome is a rare genetic disease of unknown etiology with some features suggestive of accelerated aging. Patients with this disorder are usually of average intelligence and appear clinically normal at birth. However, in early childhood they develop severe growth retardation and a senescent phenotype, including balding, aged-appe-aring skin, generalized atherosclerosis, and strokes. They die prematurely as a result... |
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- Original Article
- Clinical Studies of Brain Tumors in Children.
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In Hee Park, Han Young Lee, Jeh Hoon Shin, In Joon Seol, Woo Gill Lee, Hang Lee
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Clin Exp Pediatr. 1985;28(11):1082-1088. Published online November 30, 1985
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During a period of 116/12 years, from July, 1974 to December, 1984, 44 cases under 15 years of age with brain tumors were observed at department of pediatrics and neurosurgery at Hanyang University Hospital.
The results were as follows: 1)The peak incidence of age was observed in the children from 5 to 10 years (38.6%). The sex ratio of male to... |
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- Case Report
- A Case of Cerebral Paragonimiasis.
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Jin Young Lee, Byung Chun Suh, In Joon Seol, Heung Jae Lee, Keun Soo Lee
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Clin Exp Pediatr. 1985;28(10):1037-1041. Published online October 31, 1985
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The authors experienced a case of cerebral paragonimiasis with severe eosinophilia in a 13 year old female patient.
Since several years ago, she frequently drank spring water with her family, especially, with her father. She came to the hospital because of speech disturbance, weakness of right upper extremity and maculopapular skin rashes of lower half of body. In her family history,... |
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- Original Article
- Chromosome Study of the Congenital Anomaly and Mental Retardation in Korean Children.
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Ra Lee, In Joon Seol, Woo Gill Lee, Soo Jee Moon, Chong Moo Park
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Clin Exp Pediatr. 1981;24(9):812-819. Published online September 15, 1981
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The authors studie 111 cases of congenital anomalies and/or mental retardation. 56cases of congenital anomalies and/or mental retardations were cared and admitted at pediatric department in Han Yang University hospital. 55 cases were in institution for the mentally retarded. The authors studied chromosome analysis about 111 cases with congenital anomalies and/or mental retardation. The results obtained were as follows: A)... |
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