Bart syndrome

Bart syn·drome

(bart),
a form of epidermolysis bullosa with blistering of the extremities and intertriginous areas, congenital localized absence of skin, erosions of the mouth, and dystrophic nails; there is often spontaneous improvement with no residual scarring; autosomal dominant inheritance, caused by mutation in the collagen type VII gene (COL7A1) on chromosome 3p.

Bart syn·drome

(bahrt sin'drōm)
A form of epidermolysis bullosa with blistering of the extremities and intertriginous areas, congenital localized absence of skin, erosions of the mouth, and dystrophic nails; there is often spontaneous improvement with no residual scarring; autosomal dominant inheritance, caused by mutation in the collagen type VII gene (COL7A1) on chromosome 3p.

Bart,

Bruce Joseph, U.S. dermatologist, 1936–.
Bart syndrome - autosomal dominant trait resulting in extremity blistering, mouth erosions, and deformed nails, often with spontaneous improvement and no residual scarring.
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