Acrofacial dysostosis, Palagonia type (Q86242): Difference between revisions
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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 |
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| default for all languages | ID_656294814 |
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| 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. |
