Traditional Chinese medicine for treating Angelman syndrome

Abstract

The invention discloses a traditional Chinese medicine for treating an Angelman syndrome, and belongs to the technical field of the traditional Chinese medicine. The clinicopathologic analysis and therapeutic problems of the Angelman syndrome are solved. Analyzed by the traditional Chinese medicine viewpoint, the Angelman syndrome belongs to the inherent shortage, deficiency of the kidney and vital energy, pathogenic influence and heart spirit confused by phlegm. The traditional Chinese medicines of tonifying kidney and Qi, invigorating the circulation of blood and dispelling wind, and dissipating phlegm for resuscitation are combined as a therapeutic drug. The traditional Chinese medicine for treating the Angelman syndrome is mainly prepared by the following medicines by weight: 15 partsof fructus trichosanthis, 12 parts of bombyx batryticatus, 15 parts of the root of red-rooted salvia, 12 parts of rhizoma gastrodiae, 15 parts of radix polygonati officinalis, 15 parts of rehmannia glutinosa libosch, 13 parts of radix achyranthis bidentatae, 20 parts of crude dragon bone, 20 parts of crude ruddle, 25 parts of concha ostreae, 10 parts of uncaria, and 8 parts of rhizoma acori graminei. The traditional Chinese medicine for treating the Angelman syndrome is capable of creating a positive solution theory and a therapeutic solution of the traditional Chinese medicine for correctly analyzing the Angelman syndrome, and getting the remarkable curative effect.

Description

technical field [0001] The invention relates to a medicine for treating intractable diseases, in particular to a medicine for analyzing and treating Angelman syndrome, and belongs to the technical field of traditional Chinese medicine. Background technique [0002] Angelman syndrome (formerly known as Angelman syndrome in English), also known as Angelman syndrome, or Angelman syndrome, is a disease caused by a genetic defect. Patients suffering from this disease often have a smile on their faces, lack language skills, hyperactivity, and mental retardation. [0003] Angelman syndrome, caused by a genetic defect, is caused by a deletion of chromosome 15 q11-q13. The disease is caused by a maternal single-gene genetic defect. [0004] Clinical manifestations of Angelman syndrome: 1. It is characterized by severe dyskinesia, mental retardation, ataxia, hypotonia, epilepsy, speech impairment, and a distinctive facial appearance characterized by a large jaw, open mouth, and cry...

AI Technical Summary

Problems solved by technology

3. Some patients have motor tremor and difficulty walking, which may be caused by balance dysfunction

There is currently no cure for this condition, the symptoms can only be alleviated with age