Neurodevelopmental Disorder with Spastic Diplegia and Visual Defects

Alternative Names

  • NEDSDV
  • Mental Retardation, Autosomal Dominant 19
  • MRD19

Associated Genes

Catenin, Beta-1
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WHO-ICD-10 version:2010

Diseases of the nervous system

Cerebral palsy and other paralytic syndromes

OMIM Number

615075

Mode of Inheritance

Autosomal dominant

Gene Map Locus

3p22.1

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. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
615075.1Saudi ArabiaFemaleNoYes Motor delay; Delayed speech and language...NM_001904.4:c.999C>GHeterozygousAutosomal, DominantMonies et al. 2017
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