Thursday, September 27, 2012

General knowledge of nerve amyotrophy

General knowledge of nerve amyotrophy
General knowledge of nerve amyotrophy
General knowledge of nerve amyotrophy, these are that a lot of patients compare the question cared about, nerve amyotrophy is a kind of genetic disease, the manifestation of nerve amyotrophy mainly pains vigorously with shoulder and arm on clinic, then will also present temporary paralysis. General knowledge of nerve amyotrophy, the following contents hope it will be helpful to you. Nerve amyotrophy is a kind of rare disease, only 200 families will present this disease in the whole world. But there is HNA not hereditary either, this is called Parsonage-Turner syndrome. Have 2- 4 disease this kind of in the every 100,000 people, but clinical manifestation of them difficult to distinguish in picture and very hereditary HNA. Nerve usually by some external factor such as vaccine inoculation, infect, operation or even pregnant giving a birth, causing amyotrophy, because the danger of carrying very hereditary HNA of the apt ill physique person is very high. It causes the nerve problems around to say to be the environmental factor, so HNA is disease Parsonage-Turner syndrome Guillain-Barr that some high frequency takes place Hereditary model of syndrome. Researchers oriented HNA relevant gene after being through carrying on research to a lot of families, gene these lie mankind at the long arm of chromosome, researcher find the intersection of Septin9 and the intersection of albumen and genetic code of family of patient in the body sudden change has taken place or change 17. HNA is the first single genetic hereditary disease caused by the genetic defect of Septin family too. Researcher define the intersection of Septin9 and the intersection of albumen and function in peripheral nervous system very much at present and why HNA can produce mutant, but they other members who know Septin family relate to cell division when being formed and grown with tumour of cell skeleton. In fact it is Septin sudden change that has prevented the cell division, this can also explain why a lot of HNA patients have facial deformity. However, effective therapeutic method does not prevent or prevent nerve amyotrophy at present. After finding the relevant gene, can make and further understand the molecule mechanism of HNA disease process, and is used in the clinical treatment finally.


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