Синдром L1
ORPHA:275543· ICD-10 Q04.8· L1 syndrome
Визначення(English summary)
A rare, congenital X-linked developmental disorder characterized by hydrocephalus of varying degrees of severity, intellectual deficit, spasticity of the legs, and adducted thumbs. The syndrome represents a spectrum of disorders including: X-linked hydrocephalus with stenosis of the aqueduct of Sylvius (HSAS), MASA syndrome, X-linked complicated hereditary spastic paraplegia type 1, and X-linked complicated corpus callosum agenesis.
- Поширеність
- Unknown
- Успадкування
- X-linked recessive
- Вік початку
- Antenatal, Infancy, Neonatal