CHILD syndrome
What is CHILD syndrome?
A rare developmental defect during embryogenesis characterized by unilateral inflammatory and scaling skin lesions with ipsilateral visceral and limb anomalies.
Other condition names
- CHILD nevus
- Congenital hemidysplasia with ichthyosiform nevus and limbs defects
Inheritance type
Not applicable, X-linked dominant
Prevalence
- Worldwide: <1 in 1,000 000
Age of Onset
- Infancy
- Neonatal
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on "https://www.orphadata.com". Data version 1.3.16 / 4.1.7.