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Citrullinemia  

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Tipo

  • mesh:Descriptor

Definición

  • A group of diseases related to a deficiency of the enzyme ARGININOSUCCINATE SYNTHASE which causes an elevation of serum levels of CITRULLINE. In neonates, clinical manifestations include lethargy, hypotonia, and SEIZURES. Milder forms also occur. Childhood and adult forms may present with recurrent episodes of intermittent weakness, lethargy, ATAXIA, behavioral changes, and DYSARTHRIA. (From Menkes, Textbook of Child Neurology, 5th ed, p49)

Concepto genérico

Etiquetas alternativas

  • Argininosuccinate Synthase Deficiency Disease
  • Argininosuccinate Synthetase Deficiency
  • Argininosuccinic Acid Synthase Deficiency Disease
  • Argininosuccinic Acid Synthetase Deficiency
  • Argininosuccinic Acid Synthetase Deficiency Disease
  • ASS Deficiency
  • Citrullinuria
  • Deficiency Disease, Argininosuccinate Synthase
  • Deficiency Disease, Argininosuccinic Acid Synthase

En otras lenguas

  • francés

  • Déficit en argininosuccinate synthase
  • Déficit en argininosuccinate synthétase

URI

http://data.loterre.fr/ark:/67375/JVR-N94FJG70-H

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