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Syndromic X-linked intellectual disability Najm type
rareA rare cerebellar dysgenesis syndrome characterized by variable clinical manifestations ranging from mild intellectual deficit with or without congenital nystagmus, to severe cognitive impairment associated with cerebellar and pontine hypoplasia/atrophy and abnormalities of cortical development.
- Identifiers
- MONDO:0010417 OMIM:300749Orphanet:163937
- Also known as
- intellectual disability and microcephaly with pontine and cerebellar hypoplasia · mental retardation and microcephaly with PONTINE and cerebellar hypoplasia · mental retardation, X-linked, syndromic, Najm type · MICPCH · MICPCH syndrome
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