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Gamma-aminobutyric acid transaminase deficiency

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Description

GABA-transaminase deficiency is characterized by neonatal or early infantile-onset encephalopathy, hypotonia, hypersomnolence, epilepsy, choreoathetosis, and accelerated linear growth. Electroencephalograms show burst-suppression, modified hypsarrhythmia, multifocal spikes, and generalized spike-wave. Severity varies, but most patients have profound developmental impairment and some patients die in infancy (summary by Koenig et al., 2017).

OMIM

  • Mode of Inheritance

  • Autosomal recessive inheritance

VARIANTS

262

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Genes

External Links

  • OMIM

    613163

  • Orphanet

    2066

  • HPO
  • Medgen

    C0342708

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