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Case Report
4 Cases of Progressive Muscular Dystrophy.
Jung Hee Kim, Dong Wook Kim, Dae Deok Ahn, Jung Kwon Lee, Yoon Ja Kim
Clin Exp Pediatr. 1985;28(12):1225-1230.   Published online December 31, 1985
Progressive muscular dystropy is a genetically determined disorder characterized by-progressive weakness and wasting of skeletal muscles. The etiology of muscular dystropy is unknown, and no form of phamacological treatment is considered effective. The authors report 4 cases of P.M.D., of which 2 cases occured in a family and 2 cases were developed sporadically. They were diagnosed by clinical findings, serum,...
Original Article
Lipid Composition of Serum HDL and Fatty Acid Composition of Serum Cholesteryl Esters in Newborn.
Jung Hee Kim, Dong Wook Kim, Dae Deok Ahn, Jung Kwon Lee, Yoon Ja Kim, Jung Chull Kim, Tai Ho Chung
Clin Exp Pediatr. 1985;28(12):1190-1195.   Published online December 31, 1985
Lipid consumption in early life has been implicated with atherosclerosis in later life. It has been also claimed that lipids contents of serum in early life would reflect coronary atherosclerosis in later life. Present study has undertaken to look for the composition of serum HDL and fatty acid composition of serum cholesteryl esters in newborns. Levels of high density lipoprotein...
Case Report
Two Autopsy Cases of Pneumocystis Carinii Pneumonia.
Dae Deok Ahn, Tae Suck Jung, Jung Kwon Lee, Yoon Ja Kim
Clin Exp Pediatr. 1984;27(3):271-276.   Published online March 31, 1984
Pneumocystis infection is highly prevalent in humans and lower animals throughout the world. The disease has almost alway been sporadic, rarely epidemic, and has occurred in all age groups. We experienced two cases of pneumocystis carinii pneumonia. They were brought to our hospital from orphanage at the age of 50 day and 86 day old. The initial X-ray findings were...
A Case of Tuberous Sclerosis And Review of Literatures on 25 Cases Reported in Korea.
Yoon Ja Kim, Soo Kyung Jeong, Nam Ji Cho
Clin Exp Pediatr. 1983;26(3):290-294.   Published online March 31, 1983
We experienced a case of tuberous sclerosis who had typical triad-adenoma sebaceum, mental deficiency, and epileptic seizure-associated with hydrocephalus in 12 years old girl. We made a review of literatures on 25 cases of tuberous sclerosis which were reported in Korea.
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...
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