Synonyms: Ameloonychohypohidrotic ectodermal dysplasia | Ameloonychohypohidrotic syndrome
A rare ectodermal dysplasia syndrome characterized by the association of hypocalcified and hypoplastic tooth enamel distal finger and toenail onycholysis with subungueal hyperkeratosis and functional hypohidrosis. Additional manifestations include seborrheic scalp dermatitis and rough dry skin. Lacrymal punctae may be occasionally absent. There have been no further descriptions in the literature since 1975.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http: //www.orphadata.org. Data version October 2023.
Newly diagnosed with
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National Foundation for Ectodermal Dysplasias
The NFED mission is to empower and connect those touched by ectodermal dysplasias through education, support and research.
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
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