NESCAV Syndrome

Alternative Names

  • NESCAVS
  • Neurodegeneration and Spasticity with or without Cerebellar Atrophy or Cortical Visual Impairment
  • Mental Retardation, Autosomal Dominant 9
  • MRD9
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WHO-ICD-10 version:2010

Diseases of the nervous system

Other disorders of the nervous system

OMIM Number

614255

Mode of Inheritance

Autosomal dominant

Gene Map Locus

2q37.3

Description

NESCAV syndrome (NESCAVS) is a neurodegenerative disorder characterized by onset of features in infancy or early childhood. Affected individuals show global developmental delay with delayed walking or difficulty walking due to progressive spasticity mainly affecting the lower limbs and often leading to loss of independent ambulation. There is variably impaired intellectual development, speech delay, and learning disabilities and/or behavioral abnormalities. Additional features may include cortical visual impairment, often associated with optic atrophy, axonal peripheral neuropathy, seizures, dysautonomia, ataxia, and dystonia. Brain imaging often shows progressive cerebellar atrophy and thin corpus callosum. Some patients may show developmental regression, particularly of motor skills. The phenotype and presentation are highly variable. [From OMIM]

Epidemiology in the Arab World

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