About Progressive Familial Intrahepatic Cholestasis Type 1

Cholestasis, Progressive Familial Intrahepatic, 1, also known as byler disease, is related to cholestasis, progressive familial intrahepatic, 3 and cholestasis, progressive familial intrahepatic, 4, and has symptoms including diarrhea, icterus and pruritus. An important gene associated with Cholestasis, Progressive Familial Intrahepatic, 1 is ATP8B1 (ATPase Phospholipid Transporting 8B1), and among its related pathways/superpathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Cardiac conduction. The drugs Bile Acids and Salts and Liver Extracts have been mentioned in the context of this disorder. Affiliated tissues include liver, appendix and lung, and related phenotypes are osteopenia and hepatomegaly

Major Symptoms of Progressive Familial Intrahepatic Cholestasis Type 1

Progressive familial intrahepatic cholestasis type 1 (PFIC1), also known as non-alcoholic steatohepatitis (NASH), is a progressive autoimmune liver disease that primarily affects children. The major symptoms include persistent elevated liver enzymes, itching, and fatigue. Other symptoms may include jaundice, abdominal pain, and dark urine. Additionally, patients may experience symptoms such as insomnia, nausea, vomiting, and diarrhea.

Suitable Lifestyle for People with Progressive Familial Intrahepatic Cholestasis Type 1

The suitable lifestyle for people with Progressive familial intrahepatic cholestasis type 1 (PFIC1) includes the following points:

1. Healthy diet: PFIC1 patients need to avoid high-fat and high-cholesterol foods, such as animal fats, offal, etc. , and control carbohydrates. Compound and protein intake. It is recommended to eat more vegetables, fruits, whole grains and low-fat protein foods.

2. Moderate exercise: PFIC1 patients need to maintain moderate exercise, such as walking, jogging, swimming, etc. , to reduce the burden on the liver. Be careful not to overexert yourself and avoid strenuous exercise.

3. Stop smoking and limit drinking: PFIC1 patients should avoid smoking and drinking, as these habits can have adverse effects on the liver.

4. Weight control: PFIC1 patients need to control their weight to reduce the burden on the liver. It is recommended to achieve this through proper diet and moderate exercise.

5. Maintain a good attitude: PFIC1 patients need to maintain a good attitude and avoid excessive anxiety and pessimism in order to better cope with the disease.

6. Regular examinations: PFIC1 patients need regular examinations of liver function to ensure timely treatment of the disease. Please note that these recommendations are for guidance only and specific lifestyle changes should be tailored to individual circumstances. It is best to develop a personalized treatment and lifestyle plan under the guidance of a doctor.

Other Diseases

Progressive Familial Intrahepatic Cholestasis Type 3 Progressive Familial Intrahepatic Cholestasis Type 2 Progressive Familial Intrahepatic Cholestasis Intrahepatic Cholestasis Benign Recurrent Intrahepatic Cholestasis 1 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis, 2 Cholestasis Intrahepatic Cholecystolithiasis Progressive External Ophthalmoplegia Progressive Osseous Heteroplasia

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