About Primary Hyperoxaluria Type 1

Hyperoxaluria, Primary, Type I, also known as primary hyperoxaluria type 1, is related to primary hyperoxaluria and chromosome 2q37 deletion syndrome, and has symptoms including bone pain An important gene associated with Hyperoxaluria, Primary, Type I is AGXT (Alanine--Glyoxylate Aminotransferase), and among its related pathways/superpathways are Gene expression (Transcription) and Metabolism of proteins. The drugs Lumasiran and Pharmaceutical Solutions have been mentioned in the context of this disorder. Affiliated tissues include kidney, eye and liver, and related phenotypes are anemia and nephrocalcinosis

Major Symptoms of Primary Hyperoxaluria Type 1

Primary hyperoxaluria type 1, also known as congenital hyperoxaluria, is a rare genetic disorder that affects the kidneys and causes them to filter large amounts of urine. Some of the major symptoms of this condition include frequent urination, severe pain and discomfort when urinating, a burning sensation in the genital area, and a cloudy or strong smelling urine. Additionally, those with congenital hyperoxaluria may experience symptoms such as headaches, dizziness, and fatigue.

Suitable Lifestyle for People with Primary Hyperoxaluria Type 1

First, we need to understand what Primary hyperoxaluria type 1 is. This is a hereditary disease in which the activity of oxidase enzymes in the renal tubules of patients is reduced, leading to renal tubular dysfunction, thereby causing hyperurea azotemia and water and sodium retention. Therefore, patients need to pay special attention to their diet and treatment regimen. For patients, lifestyle modifications are critical to relieving symptoms and controlling disease progression. Here are some suggestions:

1. Control your diet: Patients need to avoid foods high in salt, protein and sugar, such as pickles, pickled foods, desserts and high-sugar drinks. At the same time, water intake should also be controlled to reduce the burden on the kidneys.

2. Vitamin supplement: Patients may be malnourished due to disease and need to supplement vitamins appropriately, such as vitamins B, C, D and K.

3. Weight control: Patients need to lose weight to reduce the burden on the kidneys. It is recommended to adopt a low-calorie, low-fat, and low-salt diet.

4. Increase potassium intake: Patients need to increase potassium intake to reduce the burden on the kidneys. This can be achieved by eating foods rich in potassium, such as bananas, spinach, beets, etc. , or by supplementing potassium salt.

5. Pay attention to rest: Patients need to maintain adequate rest to reduce the burden on the kidneys. In conclusion, for patients, lifestyle modifications are crucial to alleviate symptoms and control disease progression. It is recommended to develop a personalized treatment and lifestyle plan under the guidance of a doctor and strictly implement it.

Other Diseases

Primary Hyperoxaluria Type 3 Primary Hyperoxaluria Hyperoxaluria Primary Bone Primary Hyperparathyroidism Primary Aldosteronism Primary Macroglobulinemia Primary Erythromelalgia Various Primary and Secondary Glomerulonephritis Primary Cutaneous Amyloidosis

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