Acrofacial dysostosis, Weyers type (Q86225): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
Revision as of 11:35, 15 August 2026
Acrofacial dysostosis, Weyers type is a type of acrofacial dysostoses, a heterogenous group of disorders combining defects of limbs and mandibular/facial development. 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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_547338814 |
||
| English | Acrofacial dysostosis, Weyers type |
Acrofacial dysostosis, Weyers type is a type of acrofacial dysostoses, a heterogenous group of disorders combining defects of limbs and mandibular/facial development. 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. |
Statements
CID11:ID_547338814
0 references
dki-india-ID_547338814
0 references
Concluído
0 references
