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Pemphigus chronicus benignus familiaris
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Beschreibung:
An autosomal dominantly inherited skin disorder characterized by recurrent eruptions of vesicles and mainly on the neck, axillae, and groin. Mutations in the ATP2C1 gene (encoding the secretory pathway Ca2++/Mn2++ ATPase 1 (SPCA1)) cause this disease. It is clinically and histologically similar to - both have abnormal, unstable between and defective . It is unrelated to though it closely resembles that disease.
Synonym(s):
Hailey-Hailey-Krankheit /
Familiärer benigner chronischer Pemphigus /
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(NLM)®
(DIMDI - Deutsche Fassung)
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