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Christianson syndrome
rareA very rare form of syndromic intellectual deficit characterized by microcephaly, severe developmental delay or regression, hypotonia, abnormal movements, and early-onset seizures.
- Identifiers
- MONDO:0010278 OMIM:300243Orphanet:85278
- Causal genes
- SLC9A6
- Also known as
- Angelman-like syndrome X-linked · intellectual developmental disorder, X-linked syndromic, Christianson type · intellectual disability microcephaly epilepsy and ataxia syndrome · intellectual disability X-linked syndromic Christianson type · intellectual disability, microcephaly, epilepsy, and ataxia syndrome
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