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LETHAL EPIDERMOLYSIS BULLOSA IN BLACK SOUTH AFRICAN NEONATES
Author(s) -
BOTHWELL JANET E.
Publication year - 1996
Publication title -
international journal of dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.677
H-Index - 93
eISSN - 1365-4632
pISSN - 0011-9059
DOI - 10.1111/j.1365-4362.1996.tb03025.x
Subject(s) - medicine , epidermolysis bullosa , black african , dermatology , basement membrane , negroid , junctional epidermolysis bullosa (veterinary medicine) , pathology , epidemiology , biology , ethnology , history , biochemistry , gene , mutation
Background. While there have been a number of reports of epidermolysis bullosa (EB) occurring in South African black neonates, the disorder occurs rarely and the electron‐microscopic findings in affected South African patients have not been documented previously. Methods. All patients with neonatal EB who were biopsied for electron microscopy at the South African Institute for Medical Research between 1986 and 1992 were included in the study. The eight boys and three girls had extensive blistering and all died within the first few months of life. Results. Nine of the patients showed the features of junctional EB, whereas the remaining two were classified as dystrophic EB. There were no differences in the clinical manifestations between the two categories. Conclusions. The lethal form of EB in South African black neonates is associated with at least two types of basement membrane defect.