What is the Difference Between Glutaric Acidemia Type 1 and 2?
🆚 Go to Comparative Table 🆚Glutaric acidemia type 1 and type 2 are both inherited disorders that affect the body's ability to break down proteins and fats to produce energy. However, they are caused by different enzyme deficiencies and have distinct clinical manifestations.
Glutaric Acidemia Type 1 (GA-1):
- Caused by a deficiency of glutaryl-CoA dehydrogenase.
- Results in the accumulation of 3-hydroxyglutaric and glutaric acid.
- Symptoms include brain atrophy, macrocephaly, and acute dystonia.
- Can present with congenital anomalies, especially of the kidneys and heart.
Glutaric Acidemia Type 2 (GA-2):
- Caused by a deficiency of either electron transport flavoprotein or electron transport flavoprotein oxoreductase.
- Results in the accumulation of unused fatty acids and other harmful substances in the body.
- Symptoms include weak muscle tone, severe heart problems, and death.
- Can cause a characteristic odor resembling that of sweaty feet.
- Milder forms may only occur in times of stress, while more severe forms can manifest as a sudden episode called a metabolic crisis, characterized by acidosis and low blood glucose (hypoglycemia), causing weakness, behavior changes, and vomiting.
In summary, the main differences between Glutaric Acidemia Type 1 and Type 2 lie in the enzyme deficiencies responsible for each condition, the accumulated substances, and the specific symptoms and clinical manifestations.
Comparative Table: Glutaric Acidemia Type 1 vs 2
Glutaric acidemia types 1 and 2 are autosomal recessive genetic disorders resulting from a lack of specific enzymes. They are mainly characterized by an inability to process proteins and fatty acids properly. Here is a table summarizing the differences between the two types:
Feature | Glutaric Acidemia Type 1 | Glutaric Acidemia Type 2 |
---|---|---|
Enzyme Deficiency | Glutaryl-CoA Dehydrogenase | Electron Transfer Flavoprotein or Electron Transfer Flavoprotein Dehydrogenase |
Gene Mutations | GCDH Gene | ETFA, ETFB, and ETFDH Genes |
Symptoms | Varies, can include lesions in the basal ganglia and encephalopathic episodes | Symptoms can be mild or severe, may include congenital anomalies of the kidneys and heart |
In summary, glutaric acidemia type 1 is due to a deficiency of glutaryl-CoA dehydrogenase, while type 2 is due to a deficiency of electron transfer flavoprotein or electron transfer flavoprotein dehydrogenase. The symptoms of these disorders can vary, and the severity of the condition can also differ between individuals.
- Type I vs Type 2 Citrullinemia
- Type 1 vs Type 2 Diabetes Mellitus
- Galactosemia vs Galactokinase Deficiency
- Gluconic Acid vs Glucuronic Acid
- Alpha-Amylase vs Alpha-Glucosidase
- Glucogenic vs Ketogenic Amino Acids
- Phenylketonuria vs Galactosemia
- Ketoacidosis vs Lactic Acidosis
- Alpha vs Beta Glucose
- Galactosemia vs Lactose Intolerance
- Type 1 vs Type 2 Muscle Fibers
- Diabetes Mellitus vs Diabetic Ketoacidosis
- A1C vs Glucose
- Glycosuria vs Glucosuria
- Type 1 vs 2 Collagen
- Gestational Diabetes vs Diabetes Mellitus
- Glucose vs Galactose
- GLUT2 vs GLUT4
- Acidosis vs Acidemia