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Updated: Jan 6, 2026

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Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
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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
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.
Area of Science:
- Genetics
- Dermatology
- Molecular Biology
Background:
- Epidermolysis bullosa simplex (EBS) is a group of genetic blistering skin disorders.
- Mutations in structural proteins, particularly keratin genes like KRT5, cause EBS.
- Severe EBS forms can significantly impact quality of life.
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