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Updated: Jan 6, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
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.
Abstract:
Epidermolysis bullosa simplex (EBS) is a skin fragility disorder resulting from mutations of structural proteins in the epidermis. We provide a brief report of long-term survival and reproduction in a mother with EBS due to keratin 5 (KRT5) c.1429G > A (p.E477K) mutation, which causes a particularly severe form of the disease.
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