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Acrofacial dysostosis, Weyers type

Orpha number ORPHA952
Prevalence of rare diseases Unknown
Inheritance
  • Autosomal dominant
Age of onset Neonatal/infancy
ICD 10 code
  • Q75.4
MIM number
Synonym(s) Curry-Hall syndrome
Weyers acrodental dysostosis
Weyers acrofacial dysostosis

Summary

Acrofacial dysostoses (AFD) are a heterogenous group of disorders combining defects of limbs and mandibular/facial development. Mandibulofacial dysostosis is of varying severity, depending on the type of AFD. Acrofacial dysostosis Weyers type is a rare autosomal dominant condition of mild phenotype. Dental anomalies, nail dystrophy, postaxial polydactyly, and mild short stature are associated to a normal intelligence. Weyers syndrome and Ellis van Creveld syndrome (MIM 225500) are allelic forms of the EVC gene. Weyers and EVC syndrome generally coexist within pedigrees. Surgery may be necessary in case of polydactyly. Stomatologic follow-up is needed in the first decade. *Author: Dr J. Albuisson (January 2004)*.

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
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