GAT1 is a congenital defect that manifests by the patient not being able to break down certain amino acids.
Lactic acidemia is the presence in excess of lactic acid in blood.
Acidemia (or acidaemia) is a medical condition marked by an abnormally high concentration of hydrogen ions in a person's blood.
is it I-Valex-1, or Ketonex-1, or Neocate Infant, or Propionic acidemia
It is an organic acid produced from carbohydrate.
I presume you mean isovaleric acidemia. A characteristic sign of isovaleric acidemia is a distinctive odor of sweaty feet during acute illness. This odor is caused by the buildup of a compound called isovaleric acid in affected individuals. In other cases, the signs and symptoms of isovaleric acidemia appear during childhood and may come and go over time.
Acidosis
Alpha-imino-glutaric acid. The imino stands for a C=N double bond.
Type 1.
type 1.
Neonatal adrenoleukodystrophy , infantile Refsum disease , and hyperpipecolic acidemia involve defects in the cytoplasm organelles of cells called the peroxisomes
I believe that Type 1 is an autoimmune disease and Type 2 is not, so with Type 1 auto antibodies are present and with Type 2 they are not. Therefore, I do not believe that taking insulin can turn Type 2 into Type 1. The cause of Type 1 is still unknown.
type 1