Acrofacial dysostosis, Palagonia type (Q86242): Difference between revisions
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A disostose acrofacial, tipo palagônia, pertence ao grupo das disostoses acrofaciais, e é uma condição muito rara de gravidade leve caracterizada por baixa estatura, QI normal e disostose acrofacial leve (hipoplasia malar, micrognatia e membrana interdigital com encurtamento do quarto metacarpo) associada a oligodontia ou dentes supranumerários, anomalias vertebrais leves, defeitos de couro cabeludo ou cabelos (aplasia de cútis congênita e pelo torcido) e lábio leporino. | |||||||||||||||
| description / en | description / en | ||||||||||||||
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. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/656294814 / rank | |||||||||||||||
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CID11:ID_656294814 | |||||||||||||||
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dki-india-ID_656294814 | |||||||||||||||
| Property / Canary Token: dki-india-ID_656294814 / rank | |||||||||||||||
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| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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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 |
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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. |
Statements
CID11:ID_656294814
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dki-india-ID_656294814
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Concluído
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13 August 2026
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