'Gsd type' diaporamas de présentation

Congenital defects of carbohydrate metobolism

Congenital defects of carbohydrate metobolism. CLASSICAL GALACTOSEMIA. Defective enzyme : Galactose-1-phosphate uridyltransferase (incidence 1:40,000) Mechanism : Accumulation of galactose-1-phosphate causes intracellular ATP depletion and very toxic for liver, kidney and brain.

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By : Nur Azmina Mohd Zailan D11A025

WHAT IS GLYCOGEN STORAGE DISEASES (GSD) ?. By : Nur Azmina Mohd Zailan D11A025. GSD is the result of defects in the processing of glycogen synthesis or breakdown within muscles, liver, and other cell types. GSD has 2 classes of cause : (a) Genetic (b) Acquired.

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Glycogen Storage Diseases:

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RESEARCH PROJECT: GLYCOGEN STORAGE DISEASE TYPE I AND ATHEROSCLEROSIS

RESEARCH PROJECT: GLYCOGEN STORAGE DISEASE TYPE I AND ATHEROSCLEROSIS. a multicentre study. BACKGROUND. Glycogen storage disease (GSD) type I is characterized by hypoglycaemia, hyperuricemia, hyperlactatemia and hyperlipidemia

330 views • 13 slides