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Case Report
A Case of Incontinentia Pigmenti
Soo Young Kweon, Hyun Joo Choi, Gyung Hee Kim
Clin Exp Pediatr. 1992;35(3):417-421.   Published online March 15, 1992
Incontinentia Pigmenti is an uncommon genodermatosis that usually affects female infants. The dermatosis may be only a part of more generalized disorder which may affect with great variability the teeth, the eyes, the bones or central nervous system, or may be associated with other malformations or developmental disturbances. We experienced a case of Incontinentia Pigmenti associated with defect of a eye...
Original Article
A Case of Thanatophoric Dysplasia.
Eun Sil Kim, Hyun Joo Choi, Mi Ran Park, Jae Yun Kim, In Sang Jeon, Kwang Jeon Kim, Bum Woo Yum
Clin Exp Pediatr. 1990;33(11):1593-1597.   Published online November 30, 1990
Thanatophoric dysplasia is a short limb dwarf condition in which respiratory distress is responsible for death in the first hours or days after birth. We experienced a case of thanatophoric dysplasia who presented striking disproportion of trunk and extremities. The head was relatively large, the trunk was narrow and normal length, and the extremities were markedly shortened. The radiologic feature of this dysplasia was characteristic....
A Case of Conjoined Twins.
Hyun Joo Choi, Eun Sil Kim, In Sang Jeon, Myung Chul Cho, Kwang Jeon Kim, Nae In Lim
Clin Exp Pediatr. 1990;33(11):1562-1566.   Published online November 30, 1990
Conjoined twins is known to be very rare and to have various anatomical unions. We have experienced a case of conjoined twins which was delivered by elective Caesarian section. A case of thoracoventropagus conjoined twins is presented with brief review of literature.
A case of Idiopathic Crescentic Glomerulonephritis.
Mi Kyung Kim, Hyun Joo Choi, Seung Joo Lee, Ok Kyung Kim
Clin Exp Pediatr. 1989;32(10):1435-1441.   Published online October 31, 1989
Idiopathic crescentic glomerulonephritis is a very rare disease especially in children with poor prognosis. We experienced a case of idiopathic crescentic glomerulonephritis in a 4-year-old male patient who presented initially with a nephrotic syndrome and progressed to a rapidly progressive glomerulonephritis. We review literatures briefly.
A Case of Edward Syndrom.
Youn Hong Choi, Hyun Joo Choi, Eun Hwa Shin, Ju Hong Cha, Kwang Jeon Kim
Clin Exp Pediatr. 1989;32(3):396-401.   Published online March 31, 1989
Edward syndrome is known as 18-trisomy with multiple congenital anomalies. Recently, we experienced a case of 18-trisomy syndrome in a new-born female baby who was born at Chung Gu Sung Sim Hospital. Grossly this baby had multiple anomalies which were characterized by prominent occiput, hypertelorism, small palpebral fissure, small oral opening, high arched palate, micrognathia, low-set malformed ear, rocker bottom feet, narrow pelvis, limited...