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L1 syndrome

ORPHA:275543· ICD-10 Q04.8

Definition

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.

Prevalence
Unknown
Inheritance
X-linked recessive
Age of onset
Antenatal, Infancy, Neonatal