Acrofacial dysostosis, Palagonia type (Q86242): Difference between revisions

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Latest revision as of 11:36, 15 August 2026

Acrofacial dysostosis, palagonia type belong to the group of acrofacial dysostoses, and is a very rare condition of mild severity characterised by shortness of stature, normal IQ and mild acrofacial dysostosis (malar hypoplasia, micrognathia and webbing of digits with shortening of the fourth metacarpals) associated with oligodontia or supernumerary teeth, mild vertebral anomalies, scalp or hair defects (aplasia cutis congenita and pili torti), and cleft lip.

Language	Label	Description	Also known as
default for all languages	ID_656294814
English	Acrofacial dysostosis, Palagonia type	Acrofacial dysostosis, palagonia type belong to the group of acrofacial dysostoses, and is a very rare condition of mild severity characterised by shortness of stature, normal IQ and mild acrofacial dysostosis (malar hypoplasia, micrognathia and webbing of digits with shortening of the fourth metacarpals) associated with oligodontia or supernumerary teeth, mild vertebral anomalies, scalp or hair defects (aplasia cutis congenita and pili torti), and cleft lip.