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强直性肌营养不良症患者同胞的相对疾病严重程度。

Relative disease severity in siblings with myotonic dystrophy.

作者信息

Andrews P I, Wilson J

机构信息

Prince of Wales Children's Hospital, Sydney, Australia.

出版信息

J Child Neurol. 1992 Apr;7(2):161-7. doi: 10.1177/088307389200700205.

Abstract

Myotonic dystrophy is an autosomal dominant disorder in which an early-onset form is characteristically inherited from the mother. We studied 17 affected sibling pairs from 15 families in which two or more affected children were born to mothers with myotonic dystrophy. Later-born affected children suffered more severe disease than their first-born siblings in 13 of 17 sibling pairs. Later-born affected siblings displayed significantly more neonatal feeding difficulties, later age when first sitting alone, later age when first walking alone, and a higher incidence of scoliosis. The overall difference in disease severity between affected siblings increased as the age difference between them increased, suggesting that increasing maternal age is a factor in the relative disease severity of affected children. These findings may have relevance for genetic counseling.

摘要

强直性肌营养不良是一种常染色体显性疾病,其早发型通常由母亲遗传。我们研究了来自15个家庭的17对患病同胞,这些家庭中患有强直性肌营养不良的母亲生育了两个或更多患病子女。在17对同胞中,有13对中后出生的患病子女比其先出生的同胞病情更严重。后出生的患病同胞表现出明显更多的新生儿喂养困难、独自首次坐立的年龄更晚、独自首次行走的年龄更晚以及脊柱侧弯的发生率更高。患病同胞之间疾病严重程度的总体差异随着他们年龄差异的增加而增大,这表明母亲年龄的增加是影响患病子女相对疾病严重程度的一个因素。这些发现可能与遗传咨询有关。

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