AUTOSOMAL RECESSIVE EPIDERMOLYSIS-BULLOSA SIMPLEX - A CASE-REPORT

被引:5
作者
ABANMI, A
JOSHI, RK
ATUKORALA, DN
PEDERSEN, NB
KHAMIS, OA
机构
[1] Riyadh Armed Forces Hospital, Riyadh, 11159
关键词
D O I
10.1111/j.1365-2133.1994.tb06895.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
We report a male child with autosomal recessive epidermolysis bullosa simplex presenting at birth. The patient subsequently developed cutaneous atrophy, nail dystrophy, milia and alopecia. He had growth retardation and anaemia, but there were no other associated abnormalities. Electron microscopy showed epidermolytic cleavage. The family history indicated an autosomal recessive mode of inheritance.
引用
收藏
页码:115 / 117
页数:3
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