About Progressive Familial Intrahepatic Cholestasis Type 2

Cholestasis, Progressive Familial Intrahepatic, 2, also known as pfic2, is related to familial intrahepatic cholestasis and atp8b1 deficiency, and has symptoms including diarrhea, icterus and pruritus. An important gene associated with Cholestasis, Progressive Familial Intrahepatic, 2 is ABCB11 (ATP Binding Cassette Subfamily B Member 11), and among its related pathways/superpathways are Metabolism and Transport of inorganic cations/anions and amino acids/oligopeptides. The drug Bile Acids and Salts has been mentioned in the context of this disorder. Affiliated tissues include liver and spleen, and related phenotypes are failure to thrive and splenomegaly

Major Symptoms of Progressive Familial Intrahepatic Cholestasis Type 2

Symptoms of progressive familial intrahepatic cholestasis type 2 may include jaundice, itching, fatigue, loss of appetite, nausea, vomiting, dark urine, jaundice again, and abdominal pain.

Suitable Lifestyle for People with Progressive Familial Intrahepatic Cholestasis Type 2

The suitable lifestyle for people with Progressive familial intrahepatic cholestasis type 2 includes the following points:

1. Healthy diet: avoid high-fat, high-cholesterol, high-sugar foods, and eat more healthy foods such as vegetables, fruits, whole grains, and high-quality protein.

2. Moderate exercise: Maintaining moderate exercise, such as walking, jogging, swimming, etc. , can help reduce symptoms and improve quality of life.

3. Control weight: maintain a healthy weight, avoid obesity, and reduce the burden on the liver.

4. Avoid drinking alcohol and overeating: Drinking alcohol and overeating will aggravate the condition and be detrimental to your health.

5. Regular examinations: Go to the hospital for regular examinations to ensure that the condition is under timely control and pay attention to preventing complications.

6. Maintain a good attitude: Maintaining a good attitude and avoiding excessive anxiety, pessimism and other negative emotions will help with recovery.

Other Diseases

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

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