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Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development

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Description

Autosomal recessive peripheral neuropathy with or without impaired intellectual development is an early childhood-onset neurologic disorder characterized by slowly progressive distal motor impairment resulting in gait difficulties, often with loss of ambulation, and difficulties using the hands in most patients. Most affected individuals also have impaired intellectual development, although some have normal cognition. Electrophysiologic testing and sural nerve biopsy are most compatible with an axonal motor neuropathy; some patients may show signs of demyelination. Additional features may include eye movement abnormalities, claw hands, foot deformities, and scoliosis (summary by Ylikallio et al., 2017).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

11

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Genes

External Links

  • OMIM

    618124

  • Orphanet
  • HPO
  • Medgen

    C4748283

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