About 3-Methylglutaconic Aciduria

3-Methylglutaconic Aciduria, also known as 3-methyl glutaconic aciduria, is related to 3-methylglutaconic aciduria, type i and 3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia. An important gene associated with 3-Methylglutaconic Aciduria is OPA3 (Outer Mitochondrial Membrane Lipid Metabolism Regulator OPA3), and among its related pathways/superpathways are "Respiratory electron transport, ATP synthesis by chemiosmotic coupling, and heat production by uncoupling proteins. " and Peroxisomal lipid metabolism. Affiliated tissues include cortex, brain and pancreas.

Major Symptoms of 3-Methylglutaconic Aciduria

3-methylglutaconic aciduria (3-MAU) is an inherited metabolic disease whose main symptoms include short stature, mental retardation, unclear facial skin texture, growth retardation, and delayed sexual development. The disease usually presents symptoms in early childhood and affects both physical and mental health. 3-MAU is caused by a genetic mutation that causes the liver to be unable to metabolize 3-methylglutaconic acid (3-MA) ??normally, causing a series of symptoms. At present, the treatment of 3-MAU mainly includes dietary adjustment, drug therapy and gene therapy.

Suitable Lifestyle for People with 3-Methylglutaconic Aciduria

3-methylglutaconic aciduria (3-MAU) is an inherited metabolic disease, mainly characterized by amino acid metabolism disorders. For patients with 3-MAU, lifestyle adaptation varies between individuals, but there are some aspects that need attention.

1. Diet adjustment: 3-MAU patients need to control protein and carbohydrate intake while increasing fat intake. Patients are advised to follow a high-protein, low-fat, and low-carbohydrate diet.

2. Medication: Patients may need to receive specific medication, such as enzyme replacement therapy, gene therapy, etc. These drug treatments are usually carried out under the guidance of a professional doctor.

3. Exercise and exercise: Depending on the patient's specific condition, appropriate exercise may help improve disease symptoms. Patients should follow the advice of their doctor or professional and perform appropriate exercises.

4. Sleep and rest: Maintaining adequate sleep and rest can help the body recover and reduce disease symptoms.

5. Psychological adjustment: 3-MAU patients may face certain psychological pressure, and the support and care of family and friends are very important to the patient's recovery. It should be noted that 3-MAU is a serious disease, and patients need to strictly abide by the doctor's recommendations in every aspect of life and actively cooperate with treatment to improve the quality of life.

Other Diseases

3-Methylglutaconic Aciduria Type IV 3-Methylglutaconic Aciduria Type I Orotic Aciduria L-2-Hydroxyglutaric Aciduria D-2-Hydroxyglutaric Aciduria Glutaric Aciduria Type 3 3-Hydroxy-3-Methylglutaric Aciduria Glutaric Aciduria Type 1 Glutaric Aciduria Type 2 CblC Type Methylmalonic Aciduria and Homocystinuria

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