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Developmental and epileptic encephalopathy, 76

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Description

Developmental and epileptic encephalopathy-76 (DEE76) is an autosomal recessive neurodevelopmental disorder characterized by early-onset, usually refractory, seizures, severely delayed global development, hypotonia, peripheral spasticity, and abnormalities on brain imaging, mainly cerebral atrophy and delayed myelination. Some patients may have additional features, such as scoliosis or microcephaly. The disorder may result in death in childhood (summary by Bell et al., 2019). For a general phenotypic description and a discussion of genetic heterogeneity of DEE, see 308350.

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

15

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Genes

External Links

  • OMIM

    618468

  • Orphanet
  • HPO
  • Medgen

    C5193113

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