Hereditary spherocytosis and therapeutic drug thereof

Abstract

The invention relates to hereditary spherocytosis and a therapeutic drug thereof, belongs to the technical field of medicine and aims to solve the defects of splenectomy in surgical treatment of the hereditary spherocytosis. According to analysis, the hereditary spherocytosis is caused by congenital deficiency, liver and kidney deficiency and vital energy and blood deficiency, and patients shall take the therapeutic drug, which comprises traditional Chinese medicinal herbs with effects of tonifying spleen, liver and kidney, strengthening the essence, clearing the liver, promoting blood circulation, tonifying qi and nourishing blood, to treat the hereditary spherocytosis. The therapeutic drug comprises, by weight, 15 parts of buffalo horns, 15 parts of leeches, 20 parts of dried rehmannia roots, 10 parts of cassia seeds, 15 parts of hypericum japonicum, 15 parts of codonopsis pilosula, 10 parts of Chinese wolfberries, 18 parts of the root of bidentate achyranthes, 15 parts of turtle shells, 15 parts of astragalus membranaceus, 20 parts of yams and 7 parts of liquorice. The therapeutic drug can treat root causes of disease, has obvious therapeutic effect and is safe and stable in curative effect.

Description

technical field [0001] The invention relates to hereditary spherocytosis and a medicine for treating it, in particular to a medicine for treating traditional Chinese medicine, and belongs to the technical field of medicine. Background technique [0002] Hereditary spherocytosis is a hemolytic anemia with a congenital defect in the red blood cell membrane. The main manifestations are anemia, jaundice, and splenomegaly. The diagnosis is based on the increase in spherocytes in the blood. The way of inheritance of this disease is that both men and women can get the disease, and there will be people who get the disease in each generation, which is the so-called "autosomal dominant inheritance". The age of onset and severity of the disease vary widely, mostly in infants and childhood. If the onset occurs in newborns or infants less than 1 year old, the general condition is severe. Hereditary spherocytosis, also known as congenital hemolytic jaundice, under normal conditions, the...

AI Technical Summary

Problems solved by technology

Although splenectomy is long-lasting and effective, the spleen, as a human organ, has blood filtering function, immune function, partial hematopoietic function, blood storage function, etc. When the spleen is removed, the function of the spleen will disappear, affecting some normal physiological functions of people