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