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Syndromic X-linked intellectual disability Najm type

rare

A 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.

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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