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Article

[Hay-Wells syndrome: A case report].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie - 1 Feb 2016

Khalfi L, Hamama J, Mahroug L, Arrob A, Sabani H, El Khatib K

Abstract excerpt

Hay-Wells syndrome is a rare form of ectodermal dysplasia. We report a case of a 5-year-old girl, the daughter of non-consanguineous parents. She had the characteristic of facial dysmorphia of Hay-Wells syndrome. Molecular analysis confirmed diagnosis. The patient had a cleft palate, which is considered one of cardinal signs of this syndrome. She underwent Veau-Wardill-Kilner palatoplasty with satisfactory...

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Identifiers

PMID: 26724982
DOI: 10.1016/j.arcped.2015.11.016

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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