Spastic Paralysis, Infantile-Onset Ascending

Alternative Names

  • IAHSP
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WHO-ICD-10 version:2010

Diseases of the nervous system

Systemic atrophies primarily affecting the central nervous system

OMIM Number

607225

Mode of Inheritance

Autosomal recessive

Gene Map Locus

2q33.1

Description

Infantile-onset ascending spastic paralysis is an autosomal recessive neurodegenerative disorder characterized by onset in the first years of life of progressive upper and lower motor neuron degeneration resulting in loss of ability to walk in childhood. It initially affects the lower limbs and then ascends to the upper limbs and bulbar muscles, causing dysarthria and dysphagia. Cognition is unaffected. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
607225.1United Arab EmiratesFemaleYesYes Global developmental delay; SpasticityNM_020919.3:c.1998+42A>GHomozygousAutosomal, RecessiveSaleh et al. 2021 Similarly affected s...
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