PKU, Sorbitol, & Galactose/Fructose Disorders

Phenylketonuria (PKU) Phenylketonuria (PKU) is a genetic deficiency of either Phenylalanine Hydroxylase or its cofactor, Tetrahydrobiopterin (THB). This inhibits the conversion of Phenylalanine to …

USMLE Biochemistry High Yield Rating List

Dietary Carbohydrates and Health

Tay Sachs Disease, Gaucher & Neiman-Pick

Maltose - an overview

PKU, Phenylketonuria, Galactosemia, Hereditary Fructose Intolerance & Sorbitol Diabetic Cataracts

PKU, Sorbitol, & Galactose/Fructose Disorders

Tagatose - an overview

The genetic consequences of our sweet tooth

Clinical Approach to Inborn Errors of Metabolism in Paediatrics