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Severe intellectual disability-progressive spastic diplegia syndrome

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Description

Neurodevelopmental disorder with spastic diplegia and visual defects (NEDSDV) is characterized by global developmental delay, impaired intellectual development, axial hypotonia, and dysmorphic craniofacial features with microcephaly. Many patients have visual abnormalities, ranging from strabismus to optic nerve atrophy and retinal abnormalities. Affected individuals also develop spasticity, particularly of the lower limbs, and may have behavioral abnormalities (summary by Kuechler et al., 2015 and Kharbanda et al., 2017).

OMIM

  • Mode of Inheritance

  • Autosomal dominant inheritance

VARIANTS

22

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Genes

External Links

  • OMIM

    615075

  • Orphanet

    404473

  • HPO
  • Medgen

    C3554449

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