What is platelet dysfunction?
Thrombocytopathy is a type of blood disorder, commonly caused by genetic disorders, myeloproliferative diseases, uremia, and other reasons. Specific analyses are as follows:
1. Genetic Disorders
Thrombocytopathy is often associated with inherited genetic conditions. Gene abnormalities typically impair platelet aggregation and adhesion. Patients should strictly follow medical advice to take medications such as vitamin B12 and folic acid.
2. Myeloproliferative Diseases
Chronic myeloid leukemia and essential thrombocythemia are both types of myeloproliferative diseases that commonly lead to platelet abnormalities. Treatment usually involves taking medications such as imatinib tablets or nilotinib tablets, strictly according to medical instructions.
3. Uremia
Uremia is generally caused by long-term use of nephrotoxic drugs or extreme dieting. One of its complications may be platelet function defects. Patients should follow medical advice and take medications such as sodium bicarbonate tablets and amlodipine besylate tablets.
In addition, liver disease can also reduce the synthesis of coagulation factors, leading to conditions such as thrombocytopathy. It is important to seek timely medical evaluation at a hospital and receive treatment based on the underlying cause.