Congenital varicella syndrome
ORPHA:291· ICD-10 P35.8
Definition
A rare acquired developmental anomaly syndrome characterized by skin, neurological, ocular, limbs and growth defects secondary to maternal Varicella-Zoster Virus (VZV) infection.
- Prevalence
- Unknown
- Inheritance
- Not applicable
- Age of onset
- Antenatal, Neonatal