About Hyperhomocysteinemia

Hyperhomocysteinemia is related to homocysteinemia and homocystinuria due to deficiency of n -methylenetetrahydrofolate reductase activity. An important gene associated with Hyperhomocysteinemia is H19 (H19 Imprinted Maternally Expressed Transcript), and among its related pathways/superpathways are Metabolism and Response to elevated platelet cytosolic Ca2+. The drugs Amlodipine and Hydrochlorothiazide have been mentioned in the context of this disorder. Affiliated tissues include endothelial, kidney and smooth muscle, and related phenotypes are Increased free cholesterol and homeostasis/metabolism

Major Symptoms of Hyperhomocysteinemia

The main symptoms of Hyperhomocysteinemia include:

1. Kidney stones: Patients may experience symptoms of kidney stones, such as low back pain, hematuria, and frequent urination.

2. Hypertension: Patients with anabolic gallatinuria may develop symptoms of hypertension, such as hypertension, proteinuria, and hematuria.

3. Nervous system problems: People with anabolic gallatinuria may develop neurological problems such as headaches, insomnia, and difficulty concentrating.

4. Bone problems: Patients with anabolic gallatinuria may develop bone problems, such as osteoporosis and fractures.

5. Digestive system problems: People with anabolic gallatinuria may experience digestive system problems such as diarrhea, nausea, and vomiting.

6. Skin problems: Patients with anabolic gallatinuria may develop skin problems such as itching, rashes, and urticaria.

7. Cardiovascular problems: Patients with anabolic gallatinuria may develop cardiovascular problems, such as palpitations, irregular heartbeats, and high blood pressure. It is important to note that the symptoms of anabolic salicinuria may vary from individual to individual, and some symptoms may be related to other conditions. If you have these symptoms, please seek medical treatment promptly and receive diagnosis and treatment from your doctor.

Suitable Lifestyle for People with Hyperhomocysteinemia

Hyperhomocysteinemia (hyperhomocysteinuria) is a hereditary metabolic disease, the main feature is that the level of assimilated caricin in the urine is too high, resulting in amino acid metabolism disorder. People with Hyperhomocysteinemia should adopt the following lifestyle:

1. Control protein intake: People with Hyperhomocysteinemia should limit their intake of high-protein foods, such as meat, fish, beans, etc. , and their daily protein intake should be between Below 0. 8 g/kg body weight.

2. Increase dietary fiber intake: People with Hyperhomocysteinemia should increase dietary fiber intake to reduce the level of anabolic carnalin in urine. Foods rich in dietary fiber include fruits, vegetables, whole grains, etc.

3. Vitamin B12 supplement: People with Hyperhomocysteinemia are prone to vitamin B12 deficiency, so they need additional vitamin B12 supplements. It is recommended to take vitamin B12 supplements or foods containing vitamin B12, such as beef liver, beef kidney, etc.

4. Control the amount of alcohol you drink: People with Hyperhomocysteinemia should avoid drinking alcohol because alcohol can aggravate the condition.

5. Check your urine regularly: People with Hyperhomocysteinemia should regularly check their urine for levels of anabolic carnalin so that any kidney damage can be detected and treated early. Hyperhomocysteinemia is a serious genetic disease, so patients should consult a professional doctor as early as possible and follow the doctor's recommendations for treatment and lifestyle adjustments.

Other Diseases

Related Products