Fragile (X)(q27) sites in a pedigree with female carriers showing mild to severe mental retardation.
نویسندگان
چکیده
A pedigree showing the fragile site at Xq27 in a severely retarded female and in other less retarded carriers is described. Two of the four moderately retarded males with the fra(X)(q27) show macro-orchidism, and a variety of other features usually used to support the effects of the fra(X)(q27) are also inconsistent. A second fragile site at (10)(q23) is also present and in the two oldest females its frequency is not decreased, whereas the fra(x)(q27) is not detectable in these females although probably present. It is concluded that pedigrees showing mentally retarded females and probable X linkage should be included in studies of the fra(X)(q27).
منابع مشابه
سندرم ایکس شکننده و گزارش 3 مورد (بررسی سیتوژنیک و ملکولی)
ABSTRACT The fragile X syndrome is the most frequent cause of inherited mental retardation. The fragile site is on the long arm of X chromosome in X q27.3 region. Incidence of syndrome is 1 in 2000 in males and 1 in 2500 in females. This fragile site is visible only with using of special cultural technices. Since females have two X chromosomes, this signs apear less than males. The females who...
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Clinical diagnoses of inherited mental retardation and autism encompass heterogeneous subsets of patients with differing molecular mechanisms of disease. For simplification of molecular analysis, the study of different forms of these broader diseases makes it possible to identify a homogeneous group of patients. The molecular and genetic knowledge of fragile X syndrome (FXS) has proven valuable...
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عنوان ژورنال:
- Journal of medical genetics
دوره 19 1 شماره
صفحات -
تاریخ انتشار 1982