About Carbonic Anhydrase VA Deficiency

Carbonic Anhydrase Va Deficiency, also known as hyperammonemic encephalopathy due to carbonic anhydrase va deficiency, is related to carbonic anhydrase va deficiency, hyperammonemia due to and hypoglycemia, and has symptoms including lethargy An important gene associated with Carbonic Anhydrase Va Deficiency is CA5A (Carbonic Anhydrase 5A), and among its related pathways/superpathways is Reversible hydration of carbon dioxide. Affiliated tissues include liver and brain.

Major Symptoms of Carbonic Anhydrase VA Deficiency

Carbonic anhydrase VA deficiency symptoms include palpitations, chest pain, shortness of breath, dizziness, and fatigue.

Suitable Lifestyle for People with Carbonic Anhydrase VA Deficiency

Suitable lifestyle options for people with Carbonic anhydrase VA deficiency include:

1. Maintain adequate sleep: VA is a necessary nutrient for maintaining retinal health, and adequate sleep helps with the absorption and utilization of the vitamin.

2. Control your diet: avoid excessive intake of high-fat and high-cholesterol foods, and increase your intake of vitamin-rich foods such as vegetables, fruits, and whole grains.

3. Increase physical exercise: Proper exercise helps improve the body's immunity and the absorption and utilization of vitamins.

4. Avoid smoking and drinking alcohol: Smoking and drinking alcohol can negatively affect vitamins in the body.

5. Vitamin supplement: According to the doctor's advice, supplement vitamins A, C, E, K and other vitamins in appropriate amounts to meet the body's needs.

6. Pay attention to protecting your eyes: avoid staring at computer, mobile phone and other screens for a long time, keep an appropriate distance and avoid overexertion, which will help reduce eye fatigue and help the absorption and utilization of vitamin A.

7. Maintain a good attitude: Emotional stability and a happy mood help the absorption and utilization of vitamins, and contribute to the body's immunity and resistance.

Other Diseases

Creatine Deficiency Syndrome due to AGAT Deficiency IgA Deficiency Coenzyme Q10 Deficiency Vitamin K Deficiency 5-Oxoprolinase Deficiency HIBCH Deficiency Transcobalamin Deficiency Biotinidase Deficiency NGLY1 Deficiency Vitamin D Deficiency

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