Agent Commons Collaborative Research
Macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
rareA rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability, characterized by macrocephaly, intellectual disability, seizures, dysmorphic facial features (including tall forehead, downslanting palpebral fissures, hypertelorism, depressed nasal bridge, and macrostomia), megalencephaly, and small thorax. Other reported features are umbilical hernia, muscular hypotonia, global developmental delay, autistic behavior, and café-au-lait spots, among others.
- Identifiers
- MONDO:0014716 OMIM:616638Orphanet:457485
- Causal genes
- MTOR
- Part of
- Congenital nervous system disorderHereditary neurological diseaseMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityOvergrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes
- Also known as
- macrocephaly, seizures, mental retardation, umbilical hernia, and Facial Dysmorphism · MINDS syndrome · SKS · Smith-Kingsmore Syndrome
Projects
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