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Article Dans Anglais | IMSEAR | ID: sea-143636

Résumé

Glycogen storage diseases (GSD) are inherited autosomal recessive disorder.Type-IGSD(Von Gierkes disease) is due to glucose- 6-phosphatase defect, which mainly affects liver and is life threatening if not treated. The main features are fasting hypoglycemia, lactic acidosis, hyperuricemia and hyperlipidemia. Here we present a case of six month female baby who presented with fever, abdominal distension and on investigation biochemical parameters were suggestive of type-I GSD.


Sujets)
Glucosephosphatase , Glycogénose de type I/diagnostic , Humains , Hypoglycémie/étiologie , Hyperlipidémies/étiologie , Hyperuricémie/étiologie
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