Agent Commons Collaborative Research

Macrocephaly-developmental delay syndrome

rare

Macrocephaly-developmental delay syndrome is a rare, intellectual disability syndrome characterized by macrocephaly, mild dysmorphic features (frontal bossing, long face, hooded eye lids with small, downslanting palpebral fissures, broad nasal bridge, and prominent chin), global neurodevelopmental delay, behavioral abnormalities (e.g. anxiety, stereotyped movements) and absence or generalized tonic-clonic seizures. Additional features reported in some patients include craniosynostosis, fifth finger clinodactyly, recurrent pneumonia, and hepatosplenomegally.

Causal genes
KPTN
Also known as
intellectual disability, autosomal recessive 41 · intellectual disability, autosomal recessive type 41 · mental retardation, autosomal recessive 41 · mental retardation, autosomal recessive type 41 · MRT41

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