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Original Article
A Case of Arthrogryposis Multiplex Congenita in Identical Twin.
Chang Il An, Byeong Gu Min, Kyeng Sook Cho, Jong Dai Jo
Clin Exp Pediatr. 1990;33(10):1429-1433.   Published online October 31, 1990
Arthrogryposis Multiplex Congenita is a very rare disease of persistent joint abnormalities present at birth. We experienced a case of arthrogryposis multiplex congenita in identical twin, and a review of literature was made.
A Case of Dandy-Walker Syndrome Associated with Multiple Congenital Anomalies.
Gye Weon Shin, Chul Ho Lee, Bo Kyung Cho, Chung Sik Chun, Sung Hun Cho
Clin Exp Pediatr. 1990;33(6):848-853.   Published online June 30, 1990
The Dandy-Walker Syndrome is a developmental disorders of the brain characterized by cystic deformity of fourth ventricle, agenesis or hypoplasia of the cerebellar vermis, and hydrocephalus. This syndrome is frequently associated with central nervous system malformation and systemic anomalies. We experienced a case in a 2-day-old female who has multiple congenital anomalies. On physical examinations, macrocephaly with prominent occiput, encephalocele in the occipital area, microphth- almia,...
Two Cases of Quintuplets.
Hwa Il Kwag, Kwang Ok Lee, Wan Lee, Young Youn Choi, Tai Ju Hwang
Clin Exp Pediatr. 1989;32(5):687-694.   Published online May 31, 1989
The incidence of multiple pregnancies is realtively low in humanbeing than in other species. The reported incidence of multiple pregnancies is highest among Blacks and East Indians, followed by North European White, and is lowest among the Mongolian races. Recently, with advent of clomiphen therapy, multple pregnancies are more freqently encountered. Multiple pregnancies are frequently associated with highest rate of maternal morbidities and pregnancy wastages...
A Study on Twins.
Hyang Sook Hyun, Soon Ock Kang, Byung Hak Lim, Im Ju Kang
Clin Exp Pediatr. 1989;32(4):486-494.   Published online April 30, 1989
The incidence of twins has difference according to race, maternal age & parity, medication.history etc, especially in the dizygotic twins. Twins have poorer prognosis than singletons due to high incidece of prematurity and LBW, respiratory complications, birth trauma, congenital anomaly etc. Zygosity determination is important and done by placentatal examination, blood typing, physical similarity, HLA etc. We studied the incidence of twins and its relation...
Clinical Survey of Perinatal Mortality in Multiple Pregnancy.
Hoon Kook, Dong Hun Cho, Hwa Il Kwag, Kwang Ok Lee, Young Youn Choi
Clin Exp Pediatr. 1989;32(3):321-330.   Published online March 31, 1989
A clinical survey was performed on 151 cases of multiple pregnancies (149 cases of twins and 2 cases of triplets) and their 304 multiplets who were born at the Chonnam University Hospital during 7 years from January 1, 1980 to December 31, 1986. The results are as follows: 1) The incidence of twins was 1 out of 50 births, and that of triplets...
A Case of multiple Splenic Abscess.
J H Kim, Y H Kim, J O Lee, E R Kim, S J Lee
Clin Exp Pediatr. 1989;32(2):244-249.   Published online February 28, 1989
The authors experienced a case of multiple splenic abscess in 3 years old girl with a chief complaint of fever, anorexia and abdominal pain for 2 months. The abscess cavity was detected by abdominal ultrasonography and computerized axial tomography. Computerized axial tomography appeared as a multiple round low density areas in the spleen. Abdominal ultrasonography appeared as poorly defined focal decreased echoes in the...
Case Report
A Case of Multiple Abscesses due to Renal Stone.
Soo Ryun Choi, Choong Hyun Kim, Seung Ki Kim, Ji Sub Oh
Clin Exp Pediatr. 1985;28(12):1245-1249.   Published online December 31, 1985
We have experienced a case of multiple abscesses due to a renal stone in a 6 years-old girl who presented with, high fever, right upper quadrant tenderness and frequent vomiting. The diagnosis was made through laboratory findings, I.V.P. and operative finding. A brief review of the related literature is given.
A Case of Spontaneous Gastric Perforation in the Newborn.
Ran Suh, Gui Sook Choi, Hye Lyung Baik, Hyo Jung Kim, Sung Woo Shin
Clin Exp Pediatr. 1985;28(6):587-592.   Published online June 30, 1985
A case of multiple spontaneous gastric perforations in the premature newborn was experienced at the Han II hospital. The diagnosis was suspected by sudden abdominal distension and was estabilished by demonstration of free air in the peritoneal cavity in the plain abdominal X-ray film. The patient expired after 2 hours of abdominal distension on the first day of life. The...
A Case of Multiple Brain Abscess Complicated to Purulent Meningitis in Newborn.
Kui Ja Kim, Hye Young Chung, Tae Chan Kwon, Young Dae Kwon, Chin Moo Kang
Clin Exp Pediatr. 1983;26(7):717-721.   Published online July 31, 1983
This paper presented a case of multiple brain abscesses complicated with meningitis, found in a 7 days old newborn boy. This baby was admitted with the chief complaints of poor sucking and irritability. Diagnosis of purulent meningitis was made through CSF study. High fever and abnormal CSF(pleccytcsis and gradually increasing protein level) has been persisted inspite of broad spectrum heavy antibiotic...
A Case Report of Congenital Multiple Jejunoileal Atresia with Massive Mesenteric Defect.
Ji Young Kang, In Soon Lee, Sang Kyo Lee, Byung Wha Lee
Clin Exp Pediatr. 1983;26(3):271-274.   Published online March 31, 1983
This is a case report of congenital multiple jejunoileal atresia with massive mesenteric： defect around the ileum. He was born by mid-wife and transferred to our Dep't of Pediatrics，. In Cheon Gil Hospital on Feb. 9th’ 1981. Vomiting noted one time 17 hours after birth and abdominal film disclosed markedly geseous distention of stomach and duodenum and no gas。 in the ileum and colon....
A Case of Omphalocele Associated with Multiple Congenital Anomalies.
Yoon Ja Kim, Soo Kyung Jeong, Nam Ji Cho, Jae Keum Ji
Clin Exp Pediatr. 1983;26(1):66-70.   Published online January 31, 1983
A omphalocele associated with multiple congenital anomalies is extremely rare congenital malformation. We experienced a ruptured large omphalocele of short duration associated with multiple congenital anomalies such as patent omphalomesenteric duct, cleft palate and lip, postaxial polydactylia with dystrophic nails on both hands and leftfoot, adrenal heterotophia in left peritesticular region, pancreatic heterotophia in perisplenic lymphnode, nodular excrescene of spleen, and...
A Case of Hereditary Multiple Exostoses.
Shin Chung Jee, Keun Chul Myoung, Hyoung Ki Kim, Chang Soo Ra
Clin Exp Pediatr. 1981;24(9):897-901.   Published online September 15, 1981
The so-called "Hereditary Multiple Exostoses" disease is characterized by hard, irregular prominences appearing in the metaphyseal region of the bones. Though transmitted as an autosomal dominant trait, skipped generation are reported and presumably represent spontaneous mutations. We experienced one case of hereditary multiple exostoses of 15 years old male patient, whose father and one brother were also affected. A brief...
Original Article
A Study on Children with Dysentery-like Stool from Taegu Area in 1980.
Yong Hoon Cho, Sung Jee Nam, Ja Hoon Koo, Doo Hong Ahn, Sung Yong Seol
Clin Exp Pediatr. 1981;24(8):735-742.   Published online August 15, 1981
A clinical and laboratory study was conducted on 75 children with dysentery-like stool, who had been admitted or visited to our pediatric department, during 8 months period from January to August 1980. The following results were obtained: One to five years of age group was affected most frequently(47%), Shigella flexneri was identified by stool culture in 23 cases(30%) and Entameba...
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