molecules of the myelin sheath
No he was never cured but with Lorenzos oil the disease stopped but his mind was severly damaged and he died a day after his 31st birthday
Morquio syndrome is an inherited disease of metabolism in which the body is missing or doesn't have enough of a substance needed to break down long chains of sugar molecules called glycosaminoglycans
biochemical studies contribute to both diagnosis and treatments of disease, for understanding and maintenance of health. secondly, physiology , immunology, pharmacology ,toxicology overlaps with biochemical studies
Carol Kari has written: 'Understanding Gaucher disease' -- subject(s): Gaucher's disease, Genetic aspects, Genetic aspects of Gaucher's disease, Inborn errors of Metabolism, Metabolism, Inborn errors of, Treatment
Hurler Syndrome also known as (mucopolysaccharldosis)is a genetic disorder which is a hereditary defective gene. It is a rare, inherited disease of metabolism in which you cannot break down long chains of sugar molecules called glycosaminoglycan.
glucose metabolism
The diagnosis for Refsum disease is made based on the development of clinical manifestations and biochemical analysis detecting elevated phytanic acid in the blood.
a certain amino acid
heart attack and diabetes
Because Sandhoff disease and Tay-Sachs disease have similar clinical symptoms, distinguishing them requires biochemical analysis. This involves a test to measure enzyme activity of the two hexosaminidase enzymes.
Diabetes mellitus is the most common disorder of carbohydrate metabolism, and it is abbreviated DM.
Pathphysiology is the study of the changes of normal mechanical, physical, and biochemical functions, either caused by a disease, or resulting from an abnormal syndrome...