Generalized, severe epidermolysis bullosa simplex caused by a Keratin 5 p.E477K mutation

Sarah E Sheppard1, Laura Elizabeth Anderson2, Cathryn Sibbald2

  • 1Division of Human Genetics, Children's Hospital of Philadelphia, PA, USA.

Pediatric Dermatology
|October 4, 2019
PubMed
Summary

Epidermolysis bullosa simplex (EBS) is a rare skin disorder. This report details long-term survival and successful reproduction in a mother with a severe EBS form caused by a KRT5 gene mutation.

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