Weyers acrofacial dysostosis (Curry-Hall Syndrome): Report of a rare case

Weyers acrofacial dysostosis (Curry-Hall syndrome) is a rare autosomal dominant skeletal dysplasia manifest by nail dystrophy, oral and dental anomalies, polydactyly of the hands and feet, and mild short stature. We report an 11-year-old boy who presented with onychodystrophy, supernumerary tooth, h...

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Autore principale:	Suchetana Goswami
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Wolters Kluwer Medknow Publications 2018-01-01
Serie:	Archives of Medicine and Health Sciences
Soggetti:	Curry-Hall syndrome hypohyperdontia nail dystrophy polydactyly Weyers acrofacial dysostosis
Accesso online:	http://www.amhsjournal.org/article.asp?issn=2321-4848;year=2018;volume=6;issue=1;spage=143;epage=146;aulast=Goswami
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