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Malan overgrowth syndrome
rareA rare multisystemic genetic disorder characterized by a characteristic facial features with macrocephaly, overgrowth in infancy, intellectual disability and behavioral problems including anxieties and aggressiveness.
- Identifiers
- MONDO:0013885 OMIM:614753Orphanet:420179
- Causal genes
- NFIX
- Part of
- Hereditary diseaseMultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndromeOvergrowth syndrome
- Also known as
- Malan syndrome · Sotos syndrome 2 · Sotos syndrome type 2 · SOTOS2
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