Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 1

Alternative Names

  • PEBEL1
  • PEBEL

Associated Genes

NAD(P)HX Epimerase
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WHO-ICD-10 version:2010

Endocrine, nutritional and metabolic diseases

Metabolic disorders

OMIM Number

617186

Mode of Inheritance

Autosomal recessive

Gene Map Locus

1q22

Description

Early-onset progressive encephalopathy with brain edema and/or leukoencephalopathy-1 (PEBEL1) is an autosomal recessive severe neurometabolic disorder characterized by rapidly progressive neurologic deterioration that is usually associated with a febrile illness. Affected infants tend to show normal early development followed by acute psychomotor regression with ataxia, hypotonia, respiratory insufficiency, and seizures, resulting in coma and death in the first years of life. Brain imaging shows multiple abnormalities, including brain edema and signal abnormalities in the cortical and subcortical regions. [From OMIM]

Epidemiology in the Arab World

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Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
617186.1.1TunisiaMaleYes Generalized hypotonia; Febrile status ep...NM_144772.3:c.641T>AHomozygousAutosomal, RecessiveMaalej et al. 2022
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