Epidermolysis Bullosa Simplex: Identification of a Kindred with Autosomal Recessive Transmission of the Weher‐Cockayne Variety
作者:
Jo‐David Fine,
Lorraine Johnson,
Timothy Wright,
Yuji Horiguchi,
期刊:
Pediatric Dermatology
(WILEY Available online 1989)
卷期:
Volume 6,
issue 1
页码: 1-5
ISSN:0736-8046
年代: 1989
DOI:10.1111/j.1525-1470.1989.tb00256.x
出版商: Blackwell Publishing Ltd
数据来源: WILEY
摘要:
Abstract:With few exceptions, epidermolysis bullosa simplex (EBS) is transmitted as an autosomal dominant trait. All cases of autosomal recessive EBS reported to date have been associated with significant extracutaneous disease {including anemia, marked growth retardation, dentition abnormalities, and/or concurrent neuromuscular disease}, early infant mortality, or often, rather extensive cutaneous involvement. In some, the cutaneous morphology has even suggested junctional or dystrophic disease. We cared for a kindred in which four individuals were affected with an autosomal recessive form of EBS with cutaneous findings most often suggestive of Weber‐Cockayne disease. Except for scattered oral erosions in one patient, there was no evidence of associated extracutaneous disease. These findings demonstrate the increasing complexity of even the simplex forms of inherited epidermolysis bullosa. This obviously has implications for genetic counsellin
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