epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive

Rare Disease

MONDO:0010976

Also known as:

EBS, autosomal recessive K14EBS-AR KRT14KRT14-related autosomal recessive EBS

A basal subtype of epidermolysis bullosa simplex EBS characterized by generalized or, less frequently, localized acral blistering.

Genes

Clinical Trials

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Newborn Screening

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Patient Groups

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