Neurodegeneration with Brain Iron Accumulation 5

Alternative Names

  • NBIA5
  • Beta-Propeller Protein-Associated Neurodegeneration
  • BPAN
  • Static Encephalopathy of Childhood with Neurodegeneration in Adulthood
  • SENDA
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WHO-ICD-10 version:2010

Diseases of the nervous system

Extrapyramidal and movement disorders

OMIM Number

300894

Mode of Inheritance

X-linked dominant

Gene Map Locus

Xp11.23

Description

NBIA5, sometimes referred to as 'static encephalopathy of childhood with neurodegeneration in adulthood (SENDA) is an X-linked neurodegenerative disorder characterized by global developmental delay in early childhood that is essentially static, with slow motor and cognitive gains until adolescence or early adulthood. In young adulthood, affected individuals develop progressive dystonia, parkinsonism, extrapyramidal signs, and dementia resulting in severe disability. Brain MRI shows iron accumulation in the globus pallidus and substantia nigra. A characteristic finding is T1-weighted hyperintensity surrounding a central band of hypointensity in the substantia nigra. Cerebral and cerebellar atrophy are also observed. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
300894.1United Arab EmiratesFemaleNoYes Global developmental delay; Seizure; Int...NM_001029896.2:c.19C>THeterozygousX-linked, DominantSaleh et al. 2021 Father asymptomatic,...
300894.2United Arab EmiratesFemaleNoYes Complex febrile seizure; Global developm...NM_001029896.2:c.19C>THeterozygousX-linked, DominantMahfouz et al. 2020
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