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两个瑞典家族中的家族性X连锁智力障碍与脆性X染色体

Familial X-linked mental retardation and fragile X chromosomes in two Swedish families.

作者信息

Gustavson K H, Holmgren G, Blomquist H K, Mikkelsen M, Nordenson I, Poulsen H, Tommerup N

出版信息

Clin Genet. 1981 Feb;19(2):101-10. doi: 10.1111/j.1399-0004.1981.tb00678.x.

Abstract

X-linked mental retardation (MR) associated with a fragile X chromosome was found in two Swedish families. The fragile X chromosome was demonstrated in 5/5 boys with mental retardation. Clinical data on four of these boys are presented. In one of the families, the mental retardation was associated with macro-orchidism, large hands and large, folded ears. In the other family, macro-orchidism was not seen, possible because the boys were younger. Fragile site X chromosomes were also seen in three obligate carriers. A summary of earlier published cases of X-linked MR associated with the fragile X chromosome is given.

摘要

在两个瑞典家庭中发现了与脆性X染色体相关的X连锁智力迟钝(MR)。在5名患有智力迟钝的男孩中均发现了脆性X染色体。本文呈现了其中4名男孩的临床数据。在其中一个家庭中,智力迟钝与巨睾症、大手和大的折叠耳有关。在另一个家庭中未观察到巨睾症,可能是因为男孩们年龄较小。在3名肯定携带者中也发现了脆性位点X染色体。本文还总结了先前发表的与脆性X染色体相关的X连锁MR病例。

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