Developmental and Epileptic Encephalopathy 25 with Amelogenesis Imperfecta

Alternative Names

  • DEE25
  • Epileptic Encephalopathy, Early Infantile, 25, with Amelogenesis Imperfecta
  • EIEE25
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WHO-ICD-10 version:2010

Diseases of the nervous system

Episodic and paroxysmal disorders

OMIM Number

615905

Mode of Inheritance

Autosomal recessive

Gene Map Locus

17p13.1

Description

Developmental and epileptic encephalopathy-25 with amelogenesis imperfecta (DEE25) is an autosomal recessive neurologic disorder characterized by the onset of refractory seizures in early infancy. Most patients present with seizures in the neonatal period, which is often associated with status epilepticus. However, there is phenotypic variability, and some patients have onset of seizures later in infancy. Affected individuals show global developmental delay with intellectual disability and poor speech and communication. The seizures may remit somewhat with age, but there are persistent neurologic symptoms, including ataxia, spasticity, and abnormal involuntary movements. In addition to neurologic deficits, patients also have dental anomalies with amelogenesis imperfecta. [From OMIM]

Epidemiology in the Arab World

View Map
Subject IDCountrySexFamily HistoryParental ConsanguinityHPO TermsVariantZygosityMode of InheritanceReferenceRemarks
615905.1Saudi ArabiaMaleYesYes Microcephaly; Seizure; Hypotonia; Severe...NM_177550.5:c.1227dupHomozygousAutosomal, RecessiveMonies et al. 2017
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