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 …

Disorders of Carbohydrate Metabolism: Overview, Pathophysiological Basis of Acquired Disorders, Pathophysiology of Inherited Disorders

USMLE Step 1- Lesson 60 - Fructose and Galactose metabolism and deficiencies

Maltose - an overview

Metabolic defect in hereditary fructose intolerance. a, Fructose

2.1 Carbohydrates – Kansas State University Human Nutrition (FNDH 400) Flexbook

JaypeeDigital

JaypeeDigital

Frontiers Heterogeneity in Metabolic Responses to Dietary Fructose

IJMS, Free Full-Text

The male reproductive system in classic galactosemia: cryptorchidism and low semen volume - Gubbels - 2013 - Journal of Inherited Metabolic Disease - Wiley Online Library

My Notes for USMLE — FRUCTOSE AND GALACTOSE PATHWAYS…. AND A HARRY

Fractose and galactose Metabolism - ppt download

Nutrients, Free Full-Text

Metabolic Disorders

USMLE Step 1- Lesson 60 - Fructose and Galactose metabolism and deficiencies