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Intellectual disability-eye abnormalities-microcephaly-peripheral spasticity syndrome

ORPHA:404473· ICD-10 G80.1

Definition

A rare, genetic, syndromic intellectual disability disorder characterized by intellectual disability, significant motor delay, severe speech impairment, early-onset truncal hypotonia with progressive distal hypertonia/spasticity, microcephaly, and behavioral anomalies (autistic features, aggression or auto-aggressive behavior, sleep disturbances). Variable facial dysmorphism includes broad nasal tip with small alae nasi, long and/or flat philtrum, thin upper lip vermillion. Visual impairment (strabismus, hyperopia, myopia) is commonly associated.

Prevalence
<1 / 1 000 000
Inheritance
Unknown
Age of onset
Infancy