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12号染色体长臂24.31区至末端部分三体性

Partial trisomy 12q24.31----qter.

作者信息

Tajara E H, Varella-Garcia M, Gusson A C

出版信息

J Med Genet. 1985 Feb;22(1):73-6. doi: 10.1136/jmg.22.1.73.

Abstract

Clinical details of a male child with the karyotype 46,XY,-4,+der(4),t(4;12) (p16;q24.31)mat are reported and compared with those of other known cases of partial trisomy of the distal region of 12q. This condition is apparently associated with mental and psychomotor retardation, widely spaced eyes, flat nasal bridge, low set ears, down-turned mouth, micrognathia, loose skin at the nape, widely spaced nipples, simian creases, clinodactyly, abnormalities of the genitourinary system, alterations in the sacrococcygeal region, and deformities of the lower limbs. In the majority of the reported cases, the break-point was in the 12q24 region and resulted from adjacent 1 segregation of a maternal balanced translocation.

摘要

报告了一名核型为46,XY,-4,+der(4),t(4;12)(p16;q24.31)mat的男童的临床细节,并与其他已知的12q远端区域部分三体病例进行了比较。这种情况显然与智力和精神运动发育迟缓、眼距宽、鼻梁扁平、耳低位、嘴角下垂、小颌畸形、颈后皮肤松弛、乳头间距宽、猿掌纹、手指弯曲、泌尿生殖系统异常、骶尾区域改变以及下肢畸形有关。在大多数报告的病例中,断点位于12q24区域,是由母亲平衡易位的相邻1分离所致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da7f/1049384/c623cf3daec7/jmedgene00093-0080-a.jpg

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