Clinical phenotype of Bart's syndrome seen in a family with dominant dystrophic epidermolysis bullosa.

doi:10.1111/j.1346-8138.1998.tb02447.x

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Article

Clinical phenotype of Bart's syndrome seen in a family with dominant dystrophic epidermolysis bullosa.

The Journal of dermatology - 1 Aug 1998

Wakasugi S, Mizutari K, Ono T

Abstract excerpt

BACKGROUND: Bart's syndrome is one type of dominant dystrophic epidermolysis bullosa (EB). It is known that, in some familial cases of dominant dystrophic EB, the symptoms differ depending on the individual. We observed the way Bart's syndrome affected four generations in the same family. The pro...

Topics

Epidermolysis Bullosa Dystrophica
Humans
Infant, Newborn
Leg Dermatoses
Male
Pedigree
Phenotype
Syndrome

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