How is the plump type myocardium disease patient checked and analyze the gene? 's treatment

How is the plump type myocardium disease patient checked and analyze the gene? 's treatment
Carry on the genetic inspection to family's plump type myocardium disease patient's family members, such as the analysis on - MHC mutation gene, can find the recessive patient of the family plump type myocardium disease. Also help patient's diagnosis to establish. The scholar pays analyzing and compares with the clinical materials to two kinds of gene mutation of plump type myocardium disease of family nature, find 908Leu that has 42 who - MHC happen in a family and 195 members Val gene mutation; Greater than or equal to 17 -year-old 31 the intersection of member and competent aroused in interest to pursue, check supersound to have gene mutation to age, 19 (61%) The left thickness of room wall is greater than or equal to 13mm, 24 (77%) There are unusual electrocardiograms; 153 left thickness of room wall which does not have gene mutation members of this family are less than or equal to 12mm. The gene is checked to pursue to check easier to find the invisible plump type myocardium disease patient more aroused in interestly than the supersound. 403Arg of - MHC happen to 11 members of another family Glu gene mutation, pursues to find abnormality in electrocardiogram and supersound aroused in interest. To getting plump myocardium the intersection of disease and the intersection of family and member of patient carry on gene check, go on follow up a case by regular visits to and prophylactic treatment to gene mutation person, can reduce the incidence of dying suddenly. Sweden anyone produces and offers the chip including 12 pathogenic genes of HCM to make the genetic sieve of HCM look into and is fast, the main research direction is foundation and clinic with not normal rhythm of the heart.
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