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由于母亲的染色体易位(1q--;6p+),两名成年兄弟出现1号染色体部分三体。

Partial trisomy of chromosome no. 1 in two adult brothers due to maternal translocation (1q--;6p+).

作者信息

Taysi K, Sekhon G S

出版信息

Hum Genet. 1978 Nov 16;44(3):277-85. doi: 10.1007/BF00394292.

Abstract

Extra chromosome material on the short arm of chromosome no. 6 (46,XY,6p+) was found in two mentally retarded adult half-brothers with mildly dysmorphic features. The phenotypically normal mother had a balanced translocation between the long arm of chromosome no. 1 and the short arm of chromosome no. 6:46,XX,t(1;6)(q32;p25). Thus the two affected brothers were trisomic for the long arm segment of chromosome no. 1, distal to q 32. These patients, with mildly dysmorphic features and mental retardation, represent the first cases of partial trisomy 1q surviving to adult-hood. The clinical and cytogenetic data obtained from eight individuals with partial trisomies for different long arm segments of chromosome no. 1 suggest that partial trisomy of the distal two-thirds of the long arm in characterized by severe malformations, growth retardation, and early death. Conversely, partial trisomy for the distal one-third of the long arm is associated with milder malformations and longer survival time as well as growth and mental retardation.

摘要

在两名患有轻度畸形特征的成年智障同父异母兄弟中,发现6号染色体短臂上存在额外的染色体物质(46,XY,6p+)。表型正常的母亲在1号染色体长臂和6号染色体短臂之间存在平衡易位:46,XX,t(1;6)(q32;p25)。因此,这两名受影响的兄弟在1号染色体长臂q 32远端的片段上为三体性。这些具有轻度畸形特征和智力障碍的患者代表了首例存活至成年期的1q部分三体病例。从8名1号染色体不同长臂片段部分三体患者获得的临床和细胞遗传学数据表明,长臂远端三分之二的部分三体特征为严重畸形、生长发育迟缓及早期死亡。相反,长臂远端三分之一的部分三体与较轻的畸形、较长的存活时间以及生长发育和智力障碍有关。

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