ORPHA:235
Dubowitz syndrome
- Body system
- Bone diseases
- Inheritance pattern
- Unknown
- Typical age of onset
- Antenatal, Neonatal
- Estimated prevalence
- 1-9 / 1 000 000 (Europe)
- Rarity class
- 1-9 / 1 000 000
ORPHA:235 is classified under "Bone diseases" in the Orphanet nomenclature.
Common signs
- Microcephaly
- Hypertelorism
- Telecanthus
- Intellectual disability
- Intrauterine growth retardation
- Short stature