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Original Article
A Case of Lamellar Ichthyosis.
Yeon Seung Lim, Sang Joo Han, Won Il Park, Kyung Ja Lee
Clin Exp Pediatr. 1990;33(7):1018-1023.   Published online July 31, 1990
We observed a case of lamellar ichthyosis who was 4 day-old boy with the chief complaints of poor feeding, exessive lamellated scale covering entire body. Diagnosis of lamellar ichthyosis was estab- lished by clinical features and histopathological study. A brief review of literature was made.
A Case of Epidermolytic Hyperkeratosis.
M J Na, E W Park, W H Choi, K W Kim, D W Kim
Clin Exp Pediatr. 1990;33(5):721-726.   Published online May 31, 1990
Epidermolytic hyperkeratosis is a type of ichthyosis. We present a case of epidermolytic hyperker- atosis in 7 months old male infant who developed generalized erythematous hyperkeratosis & vesicles at birth. Later, the skin lesions progressed to characteristic thick, grayish dark brown scales affecting flexural & intertriginous areas. Histological examination revealed hyperkeratosis, vacuolation of Malpighian cells & markedly thickening of granular layer containing many keratohyaline granules.
Case Report
A Case of Collodion Baby.
Jae Gye Ryoo, Hong In Eum, Sang Cheal Lee, Jung Hee Lee
Clin Exp Pediatr. 1983;26(11):1115-1119.   Published online November 30, 1983
Ws expsrienced a ca.ss of Collodion Baby of 6 hours old female infant who was suffering from excs33ive lamellated scale, tight looking appearance and covering entire, body, typical features of parchment like skin, ectropion of upper and lower eyelids and fixed semiflexion position of the limb3. Diagnosis of Collodion Baby was established by clinical features and histopathological studies. A brief review of literature was made.
A Case of Harlequin Fetus.
Eun Hee Bak, Ai Sunn Choi, Elizabeth M Nicholson, Young Shin Kwark, Jung Hee Lee
Clin Exp Pediatr. 1981;24(10):1009-1013.   Published online October 15, 1981
The Harlequin fetus-ichthyosis fetalis-is known to be rare. Recently, we experienced a case of Harlequin fetus in stillborn infant due to autosomal recessive inheritance likely. A review of literature was done briefly.
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