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Kindler syndrome

27 Feb 2004

Abstract excerpt

Kindler syndrome is a rare, autosomal recessive skin fragility disorder characterized by blistering in infancy, followed by photosensitivity and progressive poikiloderma. Ultrastructural examination reveals marked basement membrane reduplication and variable levels of cleavage at the dermal-epidermal junction. The molecular pathology underlying Kindler syndrome has recently been shown to involve loss-of-function...

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Identifiers

PMID: 14987263
DOI: 10.1111/j.1365-2230.2004.01465.x

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