craniomicromelic syndrome
MeSH: C566522ORPHA: 1524
Overview
Craniomicromelic syndrome is a very rare disorder characterized by intrauterine growth retardation, underossification of the skull with large fontanels, short limbs with absent phalanges and finger and toe syndactyly
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Classification & Codes
MeSH Code
C566522Orphanet Code
ORPHA:1524craniomicromelic syndrome
| MeSH | C566522 |
| Orphanet | ORPHA:1524 |
| Treatments | 0 drug(s) |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO