Glutaric aciduria type II (GAII) is one of the conditions termed organic acidemias. Individuals with these conditions have a deficiency or absence of an enzyme that prevents the breakdown of certain chemicals (proteins and fats) in the body, resulting in the accumulation of several organic acids in the blood and urine.
Sep 17, 2019
Feb 1, 2014 ˇ Glutaric acidemia type II is an inherited disorder that interferes with the body's ability to break down proteins and fats to produce energy ...
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Glutaric aciduria type 2 is a rare inborn disease of fatty acid metabolism. The clinical manifestation of this disease is heterogeneous and ranges from ...
Glutaric acidemia, type II (GA-2) is a condition in which the body is unable to break down certain fats and proteins. It is considered a fatty acid ...
Sep 15, 2024 ˇ Glutaric acidemia type II is an inherited (genetic) condition that prevents the body from breaking down certain fats and proteins. Certain ...
Glutaric acidemia type 2 is an autosomal recessive metabolic disorder that is characterised by defects in the ability of the body to use proteins and fats ...
Dec 15, 2021 ˇ Glutaric acidemia type II (GA-II), also known as Multiple Acyl-Coenzyme A Dehydrogenase Deficiency (MADD), is an autosomal recessive genetic ...
Glutaric acidemia type II is an inherited metabolic disorder caused by a deficiency of either mitochondrial electron transport flavoprotein or multiple ...
Feb 1, 2014 ˇ Glutaric acidemia type II is an inherited disorder that interferes with the body's ability to break down proteins and fats to produce energy. ...
GA-2 stands for “glutaric acidemia, type 2.” People with GA-2 have problems breaking down fat and protein into energy for the body.
