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Volume 24(2); Feb 1981
Original Articles
Diagnostic Approach to Neuromuscular Disorder in Children.
Kyung Tai Whang, Shin Joong Oh, John W Benton
J Korean Pediatr Soc. 1981;24(2):101-121.   Published online February 15, 1981
The Incidence of HBs Antigenemia in Glomerular Desease and Control Group in Children.
Yong Choi, Whan Jong Lee, Jeong Kee Seo, Kwang Wook Ko
J Korean Pediatr Soc. 1981;24(2):122-127.   Published online February 15, 1981
HBsAg, HBcAb and HBsAb were examined with radio-immunoassay in 265 patients with glomerular disease, who were admitted to wards or visited to outpatient clinics of department of pediatrics, Seoul National University Hospital, from Jan., 78 to Oct. 80, and in 576 control group, with other than liver disease and without history of transfusion. The incidence in glomerular disease was 10.2%(27...
Clinical Study on Spina Bifida and Cranium Bifidum.
Hee Seon Auh, Kwan Sub Chung, Chang Jun Coe, Duk Jin Yun
J Korean Pediatr Soc. 1981;24(2):128-135.   Published online February 15, 1981
Spina bifida or cranium bifidum result from a failure in fusion of skull(cranium bifidum) or the vertebral column(spina bifida). These entities are the most common anomalies of the nervous system which are associated with major abnormalities of cellular migration, and secondary mechanical deformities of the nervous system. During the last 12 years from Jan. 1967 to Dec. 1978, 83 cases...
A Clinical Study of 15 Cases of Pneumocystis Carinii Pneumonia.
Jae Oh Kim, Sung Sook Cho, Jung Woo Suk, Don Hee Ahn, Keun Chan Sohn, Tai Hyuk Yim
J Korean Pediatr Soc. 1981;24(2):136-144.   Published online February 15, 1981
Pneumocystis carinii pneumonia is unique infection with unyielding penchant for the debilitated and immunodeficient host. Since several reports of pneumocystis carinii pneumonia in late half of 1950 period, no additional report was found in literature in Korea. We Tecently experienced 15 cases of pneumocystis carinii pneumonia in infants of an institution for foreign adoption, who, were admitted to our*hospital with...
Case Reports
Double Kidneys, Double Ureters and Ureterocele in Identical Female Twins.
Ran Namkung, Do Kwang Yun, Jun Hee Sul, Jae Seung Lee, Pyung Kil Kim, Jin Moo Lee
J Korean Pediatr Soc. 1981;24(2):145-152.   Published online February 15, 1981
We experienced a identical female twin with bilateral double kidneys, double ureters and ureterocele. Four month old baby was admitted due to high fever and irritability for 1 day. Her twin sister was also admitted two month later with the same problems. There were no abnormal findings on physical examination. Serial urinalysis revealed numerous white blood per high power field...
Fanconi Anemia.
Sang Il Lee, Young Yul Koh, Jung Gi Suh, Hyo Seop Ahn, Chang Yee Hong
J Korean Pediatr Soc. 1981;24(2):153-163.   Published online February 15, 1981
Five cases of Fanconi anemia were observed during these 7 *years. It acounts for about 6.7% of the total 75 aplastic anemia seen during those same period in SNUH. Three were boys and two were girls. The initial symptom was nasal bleeding or pallor which observed between the age of 2 years and 6 years. They all revealed growth retardation...
A Case of Short Arm Deletion of Chromosome 14.
Ra Lee, Jin Choi, Woo Gill Lee, Chong Moo Park, Yong Kyun Paik
J Korean Pediatr Soc. 1981;24(2):164-168.   Published online February 15, 1981
We have experienced a case of short arm deletion of chromosome 14 (46, XY, del (14p)) in a 3y4 years old boy who had chief problems of mental retardation and microcephaly. This case was confirmed by chromosome analysis with various banding method. Dermatoglyphic analysis of the patient showed increased total ride counts die presence of whorl patterns and simian creases...
A Case of Staphylococcal Scalded Skin Syndrome.
Jung Sook Moon, Soo Ok Lee, Dong Hwan Lee, Sang Jhoo Lee
J Korean Pediatr Soc. 1981;24(2):169-172.   Published online February 15, 1981
The authors experienced a case of staphylococcal scalded skin syndrome in 6 month old male infant and reported with brief review of literatures. His chief complaints on admission were fever, vomiting, and watery diarrhea for one day. On the fourth hospitalization day, generalized erythema was developed which was followed by generalized skin exfoliation and methicillin therapy was started. On the...
A Case of Congenital Generalized Lipodystrophy.
Woon Sik Kim, Kye Tae Kim, Don Hee Ahn, Keun Chan Sohn
J Korean Pediatr Soc. 1981;24(2):173-180.   Published online February 15, 1981
A 4 year and 2 months old girl with peculiar appearance and abdominal protuberance was prese-nted. She was the 2nd full term product of a healthy, 37-year-old mother. Any history of neonatal problems couldn’t be elicited. At 1 month of age his mother began to notice loss of subcutaneous fat with prominent musculature. At 2 months of age he was...
A Case of "Cri du Chat" Syndrome.
Jung Ho Lee, Myung Sook Lee
J Korean Pediatr Soc. 1981;24(2):181-183.   Published online February 15, 1981
"Cri du chat“ syndrome is one of rare congential chromosomal imbalance syndromes. We had experienced one case of “Cri du chat” syndrome. He had a history of frepuent U.R.I. The physical findings were characterized by cat-cryng voice, microcephaly, compartible to them of “Cri du chat” syndromd. The diagnosis was established by physical examination & chromosomal culture. A brief review of...
A Case of Anencephalus in Single-Ovum Twin.
Young Sook Hong, Young Hee Yoo, Hea Sook Kwon, Nam Ji Cho
J Korean Pediatr Soc. 1981;24(2):184-186.   Published online February 15, 1981
A case of anencephalus in single-ovum twin was observed at National Seoul Hospital and Is presented. Diagnosis of anencephalic fetus was made by abdominal Xray of mother. And a brief review on anencephalus is presented.
Problem Case Conference
Congenital syphilis with pneumonia alba and abscesses
Kwang Wouk Ko, Jae Guen Ji
J Korean Pediatr Soc. 1981;24(2):187-190.   Published online February 15, 1981
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