Baller-Gerold syndrome (Q93984): 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 09:05, 16 August 2026
Baller-Gerold syndrome is an autosomal recessive disorder characterised by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius). Patients have a predisposition to cancer, in particular osteosarcoma. B
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1650688177 |
||
| English | Baller-Gerold syndrome |
Baller-Gerold syndrome is an autosomal recessive disorder characterised by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius). Patients have a predisposition to cancer, in particular osteosarcoma. B |
Statements
CID11:ID_1650688177
0 references
dki-india-ID_1650688177
0 references
Concluído
0 references
