- Original Article
- Short-term Result of Radiofrequency Catheter Ablation in
Pediatric Patients with Paroxysmal Tachycardia
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Hee Suk Jang, Hee Jung Cho, Myung Chul Hyun, Sang Bum Lee, Young Keun Cho, Chang Ho Han
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Clin Exp Pediatr. 2000;43(2):203-209. Published online February 15, 2000
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Purpose : To find out the efficacy, safety and early complication of radiofrequency catheter ablation(RFCA) in pediatric patients with paroxysmal tachycardia, we compared short-term results of RFCA in pediatric patients to adult patients.
Methods : We studied 25 patients(11 pediatric patients, 14 adult patients), who underwent RFCA due to paroxysmal supraventricular tachycardia(PSVT) or idiopathic ventricular tachycardia(VT) from November 1997 to August... |
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- The Significance of Increased Circulating Intercellular Adhesion
Molecule 1(cICAM-1) in Neonatal Sepsis
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Hai Lee Chung, Eun Jung Park, Young Ho An, Jin Bok Hwang, Chang Ho Han, Young Dae Kwon, Sang Gyoung Kim
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Clin Exp Pediatr. 1997;40(12):1651-1659. Published online December 15, 1997
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Purpose : The early and efficient diagnosis of neonatal sepsis still remains a difficult task.
Reliable laboratory test is not available yet and treatment is mainly based on the physical
appearance of infants. And high number of negative blood cultures in cases of clinically
diagnosed sepsis further emphasize the need for a more reliable index for early diagnosis.
Intercellular adhesion molecule 1(ICAM-1) has been... |
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- A Clinical Evaluation of the Esophagogastroduodenoscopy Studies in Infants and Early Children
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Won Jung Shin, Jong Won Shin, Young Ho Ahn, Jin Bok Hwang, Chang Ho Han, Hai Lee Jung, Young Dae Kwon
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Clin Exp Pediatr. 1996;39(9):1280-1287. Published online September 15, 1996
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Purpose : Even though the causes and appearance of upper gastrointestinal tract lesions vary
with age, attention has seldomly been focused on the infancy and early childhood. This study
aimed to provide, as basic material, the experience of esophagogastroduodenoscopy(EGD) in
infants and early children.
Methods : The objects were 66 patients(male 40, female 26) who underwent EGD examination
in case of endoscopic indication at department... |
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- Intractable Diarrhea in Early Infancy : Clinical Features on Admission and A Nutritional Management
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Jong Won Shin, Kyung Won Hwang, Young Ho Ahn, Jin Bok Hwang, Chang Ho Han, Hai Lee Chung, Young Dae Kwon
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Clin Exp Pediatr. 1995;38(7):936-945. Published online July 15, 1995
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Purpose : We studied to assess the value of clinical findings on admission in screening of intractable diarrhea in early infancy(IDI) and the efficiency of early trial of semi-elemental form-ula (protein hydrolysate) as a nutritional management in IDI.
Methods : We carried out a retrospective review of medical records of twenty-eight early infants with diarrhea and malnutrition who were diagnosed as... |
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- Case Report
- Angiodysplasia Involving the Sigmoid Colon in Children
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Jae Young Kim, Kyung Won Hwang, Young Ho Ahn, Jin Bok Hwang, Chang Ho Han, Hae Lee Chung, Young Dae Kwon, Yong Jin Kim
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Clin Exp Pediatr. 1995;38(7):993-999. Published online July 15, 1995
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Angiodysplasia(AD) of the gastrointestinal(GI) tract in children is a very rare cause of bleeding and thought to be a distinct clinicopathologic entity distingishing from the classic adult-type AD by its different clinical settings and diverse histology.
We report two cases of AD involving the sigmoid colon in children. The cases, 6-year-old girl and 11-year-old boy, were preoperatively suspected by colonoscopy and... |
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- Original Article
- A Clinical Evaluation of the Gastrofiberscopy Studies in Children
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Jung Ah Park, Young Ho Ahn, Jin Bok Hwang, Chang Ho Han, Hai Lee Chung, Young Dae Kwon, Jae Bok Park
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Clin Exp Pediatr. 1995;38(11):1498-1505. Published online November 15, 1995
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Purpose : This study aimed to provide, as basic material, the experience of gastrofiberscopy in children and the clinical significance of Helicobacter pylori(H. pylori) infection in pediatric gastrointestinal disease.
Methods : The objects were 99 patients(male 49, female 50) who underwent gastrofiberscopic examination in case of endoscopic indication at department of pediatrics of Taegu Hyosung Catholic University Hospital from March 1993... |
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- A Follow-Up Study of Intractable Diarrhea in Early Infancy:
Clinical Features of Cow's Milk Allergy and Cow Milk-Sensitive Enteropathy
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Young Rak Kwon, Young Ho Ahn, Jin Bok Hwang, Chang Ho Han, Hai Lee Chung, Young Dae Kwon
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Clin Exp Pediatr. 1995;38(11):1515-1524. Published online November 15, 1995
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Purpose : The multiplicity of poorly defined illnesses and the variability of clinical and laboratory features elicited by milk ingestion in sensitized infants has made it difficult to differentiate them from the more common forms of cow milk intolerance. Following up the cases of intractable diarrhea in early infancy(illI), We investigated the clinical features of cow's milk allergy(CMA) and cow... |
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- Case Report
- Congenital Lobar Emphysema
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Cheal Gee Kim, Do Hee Choi, Jin Bok Hwang, Chang Ho Han, Hye Li Chung, Young Dae Kwon
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Clin Exp Pediatr. 1994;37(3):429-433. Published online March 15, 1994
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We had experienced a case of congenital lobar emphysema in a 3months old male infant. Chief symptoms included tachypnea, respiratory difficulty, cyanosis. Chest X-ray or chest CT scan revealed extensive emphysematous changes of the right upper and middle lobes, compression of the right lower lobe and shifted of mediastinum to the left side. This condition was appeared in the absence... |
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- Original Article
- Statistical Observation on Neonate
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Dong Il Park, Chel Gi Kim, Jin Bok Hwang, Chang Ho Han, Hye Le Chung, Young Dae Kwon
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Clin Exp Pediatr. 1993;36(8):1080-1093. Published online August 15, 1993
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A statistical obsevation was performed on 13,317 cases of neonates who had been delivered at Taegu Catholic Hospital during the past 3 years from Jan. 1 st 1988 to Dec. 31 st 1990.
The results obtained were as follows:
1) Among 13,317 neonates, the male was 7,234 and the femlae 6,083, with the sex ratio of male to female being 1.19:1
2) Percentage... |
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- Case Report
- A Case of Colodion Bady
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Dong Il Park, To Hyi Choi, Jin Bok Hwang, Chang Ho Han, Hye Li Chung, Young Dae Kwon
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Clin Exp Pediatr. 1993;36(6):858-864. Published online June 15, 1993
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This is a rare typical case of collodion baby: The patient is a one-day-old newborn male who has been suffering from the tightly collodion or parchment-like coverings over the entire skin surface with ectropion, eclabion, fixed semiflexion position of the limbs and fissures on the flexual area. The family history was noncotributory with no consanguinity. This patient was desquamted from... |
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- Original Article
- Statistical Study of Accidental Pediatric Patients in Emergency Room
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Hyo Jeong Kim, Kwang Ik Song, Jin Bok Hwang, Chang Ho Han, Hye Li Chung, Young Dae Kwon
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Clin Exp Pediatr. 1992;35(5):621-629. Published online May 15, 1992
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This study was designed to evaluate the prevalence and significant features of 3,234 pediatric accidental patients who visited emergency room during 6 years period from January 1982 to December 1987.
1) The accidental pediatric patients were 26.7% of total pediatric patients who visited emergency room The frequency of Childhood accidents was increased in later 2 years period(34.7%) compared with the early... |
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- Case Report
- A Case of 8q2 Trisomy
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Kwang Ik Song, Hyo Jeoing Kim, Jin Bok Hwang, Chang Ho Han, Hye Li Chung, Young Dae Kwon
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Clin Exp Pediatr. 1992;35(5):718-722. Published online May 15, 1992
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A case of 8q2 trisomy with mental retardation and mutiple congenital anomalies has been presented with the review of related literatures. The patient was 6 month old male child with mild mental and growth retardation, microcephaly, flat occiput, hypertelorism, broad and flat nose, low-set and promient cupped ears, micrognathia, short and wide neck, widely spaced nipples, thoracolumbar scoliosis, single transverse... |
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- Original Article
- Two cases of Edward syndrome.
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Jin Bok Hwang, Woo Hyun Kwon, Soon Young Song, Chang Ho Han, Hye Li Chung, Young Dae Kwon
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Clin Exp Pediatr. 1991;34(2):250-255. Published online February 28, 1991
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We presented two cases of Edward syndrome in this report.
Both cases were bom with multiple congenital malformation which were characterized by low set
malformed ears, micrognathia, webbed neck, rocker bottom feet, small pelvic and abducted, index
and third fingers flexed upon with simian crease and small sized great toes with mild dorsifiexion.
A large VSD was found on autopsy in one case who... |
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- A case of incontinentia pigmenti.
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Kwang Ik Song, Hyo Jeong Kim, Jin Bok Hwang, Chang Ho Han, Hye Li Chung, Young Dae Kwon
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Clin Exp Pediatr. 1991;34(10):1446-1451. Published online October 31, 1991
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A case of incontinentia pigmenti, Bloch-Sulzberger type, without any developmental defect has
been presented with the review of related literatures.
The patient was a 4 day-old female infant with irregular, grouped vesicobullous lesions on the
whole body, especially on the trunk and extremities since birth.
No familial traits was noted.
Diagnosis was made by the charateristic clinical, labaratory and histopathologic findings. |
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- Transient symptomatic zinc deficiency in a breast-fed, post term infant.
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Jin Bok Hwang, Soon Young Song, Woo Hyun Kwon, Chang Ho Han, Hye Li Chung, Young Dae Kwon
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Clin Exp Pediatr. 1991;34(1):101-106. Published online January 31, 1991
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Acrdermititis enteropathica is a rare autosomal recessive disorder of zinc absorption and its
cardinal symptoms appear at the time of weaning from breast milk which has been referred to as
most appropriate formula to prevent and treat this disease.
However, recent reports presented Transient Symptomatic Zinc deficiency (TSZD) in infants fed
breast milk whom they treated with transitory zinc supplement with no recurrence.
We experienced... |
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- A Case of Congenital Hypothyroidism.
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Woo Hyon Kwon, Soon Young Song, Chang Ho Han, Hyae Ri Chung, Soo Yong Kim, Young Dae Kwon
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Clin Exp Pediatr. 1990;33(5):708-713. Published online May 31, 1990
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Recently, we experienced a case of congenital hypothyroidism in 3month-old girl, who came with
chief complaints of prolonged jaundice for 2 months after birth.
After admission, she was diagnosed congenital hypothyroidism by the laboratory tests, including
biochemistry, radioimmunoassay, radioisotope study, and bony radiography, and since then treated
with sodium-L-thyroxine orally.
The case was presented with brief review of literatures. |
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- Case Report
- A Case of Epidermolysis Bullosa Letalis.
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Sang Taek Lee, Chang Ho Han, Soo Young Kim, Jung Kwon Lee, Young Dae Kwon, Han Ik Bae
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Clin Exp Pediatr. 1987;30(7):818-825. Published online July 31, 1987
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Epidermolysis bullosa letalis is an uncommon skin disease which is manifest at birth or in infancy.
It is characterized by blister formation occurring spontaneously or after friction or slight trauma.
This blistering disorder has the most severe clinical course, so that death may occur in infancy.
Recently, we experienced a case of epidermolysis bullosa letalis in one day old newborn infant, who
was developed... |
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- Original Article
- Seven Autopsy Cases of Anencephaly.
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Sang Taek Lee, Chang Ho Han, Soo Yong Kim, Jung Kwon Lee, Young Dae Kwon
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Clin Exp Pediatr. 1987;30(11):1318-1322. Published online November 30, 1987
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We experienced 7 cases of the anencephaly, 6 males and 1 female neonates. Their external
appearances were quite normal and relatively well developed except acranias, but all cases had
some developmental deficiency of visceras. A brief review of literature was made.
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