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Intellectual disability-early-onset cataract-microcephaly syndrome

ORPHA:633035· ICD-10 Q87.8

Definition

A rare multiple congenital anomalies/dysmorphic syndrome characterized by severe intellectual disability, global developmental delay with no speech (some patients may have limited speech), inability or difficulty to walk, microcephaly, and early-onset cataract. Additional clinical features may include hypotonia, spasticity, endocrine/metabolic diseases and immunodeficiency with lymphopenia.

Prevalence
<1 / 1 000 000
Age of onset
Infancy