Синдром CHILD
ORPHA:139· ICD-10 Q87.8· CHILD syndrome
Визначення(English summary)
A rare developmental defect during embryogenesis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies.
- Поширеність
- <1 / 1 000 000
- Успадкування
- X-linked dominant
- Вік початку
- Antenatal, Infancy, Neonatal