About Glutathione Synthetase Deficiency

Glutathione Synthetase Deficiency, also known as pyroglutamic aciduria, is related to hemolytic anemia and bilirubin metabolic disorder, and has symptoms including abdominal pain, diarrhea and vomiting. An important gene associated with Glutathione Synthetase Deficiency is GSS (Glutathione Synthetase), and among its related pathways/superpathways are Metabolism and Metapathway biotransformation Phase I and II. Affiliated tissues include brain, neutrophil and bone marrow, and related phenotypes are hemolytic anemia and abnormality of immune system physiology

Major Symptoms of Glutathione Synthetase Deficiency

Glutathione synthetase deficiency is a rare genetic disorder that affects the production of the immune system's natural protector, glutathione. The major symptoms include anemia, fatigue, recurrent infections, and rashes.

Suitable Lifestyle for People with Glutathione Synthetase Deficiency

Suitable lifestyle options for people with Glutathione synthetase deficiency include:

1. Adjust dietary habits: ensure adequate intake of protein, vitamins and minerals, especially grains, vegetables and fruits. Reduce your intake of excess fat and sugar.

2. Moderate exercise: Moderate aerobic exercise can help maintain physical health and strengthen the immune system.

3. Manage stress: Learn ways to cope with stress, such as deep breathing, meditation and relaxation exercises, to reduce the negative effects of stress on the body.

4. Maintain good sleep quality: Make sure you get enough sleep every day to help your body recover and repair.

5. Avoid smoking and drinking: These habits can have a negative impact on your health and increase your risk of illness.

6. Supplement essential amino acids: For people suffering from Glutathione synthetase deficiency, supplementing essential amino acids may help improve physical health. Please note that these recommendations are for reference only and specific recommendations should be based on individual circumstances and physician advice.

Other Diseases

Creatine Deficiency Syndrome due to AGAT Deficiency IgA Deficiency Protein S Deficiency Vitamin A Deficiency Prolidase Deficiency GATA2 Deficiency Tetrahydrobiopterin Deficiency Protein C Deficiency Proopiomelanocortin Deficiency LRBA Deficiency

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