CHILD syndrome
ORPHA:139· ICD-10 Q87.8
Definition
A rare developmental defect during embryogenesis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies.
- Prevalence
- <1 / 1 000 000
- Inheritance
- X-linked dominant
- Age of onset
- Antenatal, Infancy, Neonatal