Clinical manifestations of hereditary triple positive

For many people, hereditary triple positive is a genetic disease that causes great harm to the liver. Therefore, many patients with hereditary triple positive want to fully understand the clinical manifestations of hereditary triple positive in order to recover as soon as possible. The following content provides specific answers, so that many patients with this genetic disease can have a comprehensive understanding of the clinical manifestations.

1. Chronic HBV carriers are mostly asymptomatic and are often in the immune tolerance period. Except for the "big three positives" and positive virus tests, other growth indicators and even pathological indicators are normal. Although no drug treatment is required during this period, regular testing and observation are required to detect disease progression in time. Studies on carriers have also shown that a small number of carriers have normal liver function, but the disease still progresses. After several years, it can also progress to hepatitis, cirrhosis and even liver cancer. Therefore, regular check-ups are required to detect disease progression in time and intervene in time.

2. Chronic hepatitis B: It can be divided into three types: mild, moderate and severe according to the condition.

Mild: The condition is relatively mild, with recurrent symptoms of fatigue, dizziness, loss of appetite, aversion to oil, yellow urine, discomfort in the liver area, poor sleep, slightly enlarged liver with slight tenderness, and mild splenomegaly. Some cases have no symptoms or signs. Only 1 or 2 liver function indicators were slightly abnormal.

Moderate: Symptoms, signs, and laboratory tests are between mild and severe.

Severe: There are obvious or persistent symptoms of hepatitis, such as fatigue, poor appetite, abdominal distension, yellow urine, loose stools, etc., accompanied by liver disease face, liver palms, spider nevi, splenomegaly, repeated or persistent increase in ALT and/or aspartate aminotransferase (AST), decreased albumin, and significantly increased immunoglobulin G.

This article introduces in detail the clinical manifestations of hereditary triple positive. For some patients with this genetic disease, in order to recover as soon as possible, after fully understanding the above clinical manifestations, in order to recover as soon as possible through treatment, they must go to a large hospital for a comprehensive examination, and receive correct treatment after the examination to recover as soon as possible.