Peripheral Neuropathy, Autosomal Recessive, with or without Impaired Intellectual Development

Alternative Names

  • PNRIID
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WHO-ICD-10 version:2010

Diseases of the nervous system

Polyneuropathies and other disorders of the peripheral nervous system

OMIM Number

618124

Mode of Inheritance

Autosomal recessive

Gene Map Locus

21q22.3

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. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
603294.1.1LebanonFemaleYesNo Distal muscle weakness; Foot dorsiflex...NM_003906.5:c.2609T>CHomozygousAutosomal, RecessiveKennerson et al. 2018
603294.1.2LebanonMaleYesNo Distal muscle weakness; Foot dorsiflexo...NM_003906.5:c.2609T>CHomozygousAutosomal, RecessiveKennerson et al. 2018 Sibling of 603294.1....
603294.1.3LebanonFemaleYesNo Distal muscle weakness; Foot dorsiflexo...NM_003906.5:c.2609T>CHomozygousAutosomal, RecessiveKennerson et al. 2018 Sibling of 603294.1....
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