Glutaric aciduria type 1 (GA1) is a rare but serious inherited condition. It means the body can't process certain amino acids ("building blocks" of protein), causing a harmful build-up of substances in the blood and urine. Normally, our bodies break down protein foods like meat and fish into amino acids.
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Sep 1, 2019 ˇ It is classified as an organic acid disorder, which is a condition that leads to an abnormal buildup of particular acids known as organic acids.
Glutaric aciduria type I (GA1) is a rare hereditary metabolic disorder caused by a deficiency of the mitochondrial enzyme glutaryl-CoA dehydrogenase (GCDH). It ...
Glutaric aciduria type I (synonym, glutaric acidemia type I) is an autosomal recessive disease caused by inherited deficiency of glutaryl-CoA dehydrogenase ( ...
Jun 14, 2022 ˇ Glutaric aciduria type 1 (GA1) is a rare neurometabolic disorder that can lead to encephalopathic crises and severe dystonic movement ...
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 ...
Sep 17, 2019 ˇ GAII is an autosomal recessive genetic disorder caused by mutations in the ETFA, ETFB, or ETFDH genes. Treatment varies depending on the ...
Glutaric acidemia type 1 (GA-1) is an inherited condition caused by a faulty gene. In children with GA-1, an enzyme that helps the body process amino acids ...
Glutaric acidemia type 1 (GA1) is an inherited disorder in which the body is unable to completely break down the amino acids lysine, hydroxylysine and ...
Glutaric acidemia (GA) represent a group of genetic disorders characterized by excessive and pathological organic acid accumulation in urine and intermediates ...
