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Familial anetoderma
rareFamilial anetoderma is an extremely rare genetic skin disease characterized by loss of elastin tissue leading to localized areas of flaccid skin and a family history of the disorder.
- Identifiers
- MONDO:0016445 Orphanet:228277
- Part of
- Dermis disorder
- Also known as
- hereditary anetoderma · hereditary macular atrophy
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