- Case Report
- A Case of Incontinentia Pigmenti
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Soo Young Kweon, Hyun Joo Choi, Gyung Hee Kim
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Clin Exp Pediatr. 1992;35(3):417-421. Published online March 15, 1992
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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... |
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- Original Article
- A Case of Thanatophoric Dysplasia.
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Eun Sil Kim, Hyun Joo Choi, Mi Ran Park, Jae Yun Kim, In Sang Jeon, Kwang Jeon Kim, Bum Woo Yum
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Clin Exp Pediatr. 1990;33(11):1593-1597. Published online November 30, 1990
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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.... |
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- A Case of Conjoined Twins.
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Hyun Joo Choi, Eun Sil Kim, In Sang Jeon, Myung Chul Cho, Kwang Jeon Kim, Nae In Lim
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Clin Exp Pediatr. 1990;33(11):1562-1566. Published online November 30, 1990
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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. |
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- A Case of Edward Syndrom.
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Youn Hong Choi, Hyun Joo Choi, Eun Hwa Shin, Ju Hong Cha, Kwang Jeon Kim
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Clin Exp Pediatr. 1989;32(3):396-401. Published online March 31, 1989
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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... |
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- A case of Idiopathic Crescentic Glomerulonephritis.
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Mi Kyung Kim, Hyun Joo Choi, Seung Joo Lee, Ok Kyung Kim
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Clin Exp Pediatr. 1989;32(10):1435-1441. Published online October 31, 1989
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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. |
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