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Original Article
A Case of Encepahlocele.
Young Zong Oh, Cheol Hee Hwang, Young Ha Kim, Moon Kee Cho, I.H. Kim, S.N. Hong, J.H. Kim
Clin Exp Pediatr. 1990;33(10):1423-1428.   Published online October 31, 1990
Encephaloele which generally denotes a cephalic hernia through a congenital defect in the skull is relatively frequent congenital malformation whose incidence has been estimated at one in every 3,000 to 10,000 live births. The great majority of encephaloceles are located in the occipital area. Three- quarters of the childen with occipital encephaloceles are females. We have experienced a one day old girl who had...
A Case of Prune Belly Syndrome.
Myoung Suk Nam, Soon Soen Lim, Young Ha Kim, Moon Ki Joe
Clin Exp Pediatr. 1989;32(6):852-856.   Published online June 30, 1989
We have recently experienced a case of prune.belly syndrome in 1.day.old male with congenital defect of abdominal muscles, both cryptorchidism, ureter and bladder dilatation, left renal cyst. Imperforate anus and left club foot were associated. The diagnosis was confirmed by autopsy. A brief review of Iiterature was made.
Two Cases of Osteogenesis Imperfecta Congenita.
Soon Soen Lim, Byeung Ho Lee, Young Ha Kim, Moon Ki Joe
Clin Exp Pediatr. 1988;31(8):1085-1090.   Published online August 31, 1988
Osteogenesis imperfecta is an inherited disorder of connective tissue that affects the skeleton, ligament, skin, sclerae and dentin. It is thought to be characterized by the abnormal maturation of collagen in both mineralized and nonmineralized tissues. The three major clinical criteria are osteoporosis with abnormal fragility of the skeleton, blue sclerae and dentinogenesis imperfecta. The presence of two of these abnormalities confirms the diagnosis. We have...
A Case of Cloacal Extrophy.
Byung Ho Lee, Soon Seon Lim, Young Ha Kim, Moon Ki Cho
Clin Exp Pediatr. 1988;31(3):404-409.   Published online March 31, 1988
Cloacal exstrophy is an extremly rare and curious anomaly that involves not only the genitourinary system but also the intestinal tract, resulted from the abnormaly large cloacal membrane and its early dehiscence. The authors experienced a case of cloacal exstrophy in one day old neonate whose intestine and bladder were exstrophied and showed omphalocele, imperforated anus and meningocele. Radiologic examination revealed widely separated symphysis pubic...
Case Report
A Case of Hereditary Spherocytosis.
Yeon Kyun Oh, Byeong Ho Lee, Young Ha Kim, Moon Ki Cho
Clin Exp Pediatr. 1986;29(9):1021-1027.   Published online September 30, 1986
We experienced a case of hereditary spherocytosis in a 6 year 3 month old boy who complained of anemia and jaundice. The diagnosis was confirmed by spherocytes in peripheral blood, osmotic fragility test, autohemolysis test and bone marrow smear. This patient had a splenectomy and was discharged in good health. To date no complic ation has been detected. A brief review...
A Case Ritter's Disease.
Hwan Jong Kim, Young Ha Kim, Kyu Cha Kim
Clin Exp Pediatr. 1978;21(11):817-820.   Published online November 30, 1978
We experienced a patient of 13 days old female who was diagnosed with Ritter's disease and reported with brief review of literatures. 3 days before entry, she was suffered from fever, irritability and bullous skin lesions suddenly. And then coagulase-positive staphylococcus aureus was isolated from skin lesions and treated with systemic and local supportive measures.
A Case of Sclerema Neonatorum.
Young Ha Kim, Sung Bae Park, Kyu Cha Kim
Clin Exp Pediatr. 1978;21(2):148-151.   Published online February 28, 1978
We were experienced a case of sclerema neonatorum which was developed in a 13 days old newborn, and we report it with a brief review.
A Case of Cryptococcal Meningitis
Young Chui Moon, Young Ha Kim, Kyu Cha Kim
Clin Exp Pediatr. 1976;19(4):291-294.   Published online April 30, 1976
We were experienced a case of cryptococcal ^meningitis in 5 years old girl that similar to tuberculous meningitis on course and laboratory examination, at first. And we report with brief review of the related literature.