Tel Hashomer camptodactyly syndrome
MeSH: C536953ORPHA: 3292
Overview
Tel Hashomer camptodactyly syndrome is a rare syndrome characterized by camptodactyly, muscle hypoplasia and weakness, skeletal anomalies, facial dysmorphism and abnormal dermatoglyphics
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C536953Orphanet Code
ORPHA:3292Tel Hashomer camptodactyly syndrome
| MeSH | C536953 |
| Orphanet | ORPHA:3292 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO