About Prolidase Deficiency

Prolidase Deficiency, also known as hyperimidodipeptiduria, is related to paroxysmal extreme pain disorder and splenomegaly, and has symptoms including petechiae of skin An important gene associated with Prolidase Deficiency is PEPD (Peptidase D). Affiliated tissues include skin, spleen and liver, and related phenotypes are hearing impairment and depressed nasal bridge

Major Symptoms of Prolidase Deficiency

Prolidase deficiency is a rare genetic disorder that primarily affects the breakdown of food particles in the digestive system. The major symptoms include difficulty swallowing food, chronic constipation, vomiting, diarrhea, abdominal pain, and weight loss.

Suitable Lifestyle for People with Prolidase Deficiency

The suitable lifestyle for people suffering from Prolidase deficiency includes the following points:

1. Maintain adequate nutrition: Prolidase deficiency will cause the body's ability to absorb and utilize certain nutrients to decrease, so patients need to consume sufficient protein, vitamins and minerals. substances to maintain good health.

2. Control the fiber in the diet: Prolidase deficiency will cause the fiber in the intestines to be unable to be effectively broken down, thus aggravating symptoms. Therefore, patients should avoid eating high-fiber foods such as fruits, vegetables, whole grains, and legumes.

3. Increase carbohydrate intake: Prolidase deficiency will affect the body's absorption and utilization of carbohydrates, so patients need to increase carbohydrate intake appropriately to ensure sufficient energy and physical strength.

4. Pay attention to a balanced diet: Patients need to maintain a balanced diet and avoid over-reliance on a certain type of food to ensure the body's effective absorption and utilization of various nutrients.

5. Maintain appropriate exercise: Proper exercise helps improve the body's absorption and utilization of nutrients and helps reduce symptoms. Patients can choose low-intensity, aerobic exercise, such as walking, jogging, swimming, etc.

6. Get regular check-ups: Prolidase deficiency is a hereditary disease, and patients need regular check-ups to ensure that the disease is diagnosed and treated in a timely manner.

7. Follow the doctor's advice: If the patient is diagnosed with Prolidase deficiency, he should follow the doctor's advice and strictly follow the medication.

Other Diseases

Creatine Deficiency Syndrome due to AGAT Deficiency IgA Deficiency Coenzyme Q10 Deficiency Vitamin D Deficiency 5-Oxoprolinase Deficiency HIBCH Deficiency Transcobalamin Deficiency Biotinidase Deficiency Vitamin B12 Deficiency NGLY1 Deficiency

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