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5-OXOPROLINURIA [1 record]

Record 1 2006-01-12

English

Subject field(s)
  • Symptoms (Medicine)
  • Endocrine System and Metabolism
CONT

The phenotypic manifestations that have been described in association with GS [glutathione synthetase deficiency] deficiency include hemolytic anemia (occurring in mild GS deficiency) and 5-oxoprolinuria (pyroglutamicaciduria) and variable degrees of secondary neurological involvement (occurring in systemic GS deficiency).

French

Domaine(s)
  • Symptômes (Médecine)
  • Systèmes endocrinien et métabolique
DEF

Maladie métabolique héréditaire récessive autosomique caractérisée par l'accumulation et l'excrétion urinaire excessive d'acide pyroglutamique (5-oxoproline), due au défaut de l'activité de la glutathionsynthétase.

CONT

Le déficit en 5-oxoprolinase est une maladie autosomique récessive très rare [...] Le diagnostic est établi par la présence de 5-oxoprolinurie et par la faible activité de la 5-oxoprolinase.

OBS

Elle entraîne une anémie hémolytique chronique et une acidose métabolique, cette dernière pouvant faire défaut.

Key term(s)
  • 5 oxoprolinurie

Spanish

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