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GTR Home > Conditions/Phenotypes > Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism

Summary

Neurodevelopmental disorder with motor abnormalities, seizures, and facial dysmorphism (NEDMSF) is characterized by global developmental delay, poor overall growth, early-onset seizures (in most patients), severely impaired motor development with hypotonia and/or ataxia, and dysmorphic facial features. Affected individuals have impaired intellectual development, which can be severe. Brain imaging may show thin corpus callosum, enlarged ventricles, or cerebellar atrophy (Gennarino et al., 2018; Voet et al., 2020). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: HSPUM, NEDMSF, PUMH, PUMH1, PUML1, SCA47, PUM1
    Summary: pumilio RNA binding family member 1

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