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一名患有非梗阻性无精子症、身材矮小和骨骼缺陷的年轻男性,其Y染色体长臂和近端短臂重复,几乎所有PAR1(包括SHOX)缺失。

Duplication of Yq- and proximal Yp-arms with deletion of almost all PAR1 (including SHOX) in a young man with non-obstructive azoospermia, short stature and skeletal defects.

作者信息

Cancemi Dino, Iannuzzi Alessandra, Perucatti Angela, Montano Luigi, Capozzi Oronzo, Spampanato Carmine, Ventruto Maria Luisa, Urciuoli Maria, Iannuzzi Leopoldo, Ventruto Valerio

机构信息

Ricerche e Diagnosi Genetiche Cancemi, Corso Vittorio Emanuele, Naples, Italy.

Institute of Animal Production Systems in Mediterranean Environments (ISPAAM), Laboratory of Cytogenetics, National Research Council (CNR) of Italy, Via Argine, 1085, 80147, Naples, Italy.

出版信息

J Appl Genet. 2017 Nov;58(4):481-486. doi: 10.1007/s13353-017-0412-7. Epub 2017 Oct 6.

Abstract

Duplications of Yq arm (and AZF) seems to be tolerated by fertile males, while mutations, deletions, duplications or haploinsufficiency of SHOX can originate a wide range of phenotypes, including short stature and skeletal abnormalities. We report a case of non-obstructive azoospermia in a young man with short stature, skeletal anomalies, normal intelligence and hormonal parameters. This male showed a very singular Y-chromosome aberration, consisting of a duplication of Yq and proximal regions of Yp, with a deletion of almost all PAR1 in Yptel, including SHOX. CBA- and RBA-banding and FISH-mapping with telomeric, centromeric, AZF and SHOX probes were used. These results were confirmed by array CGH, which revealed the following karyotype constitution: arr [hg19] Xp22.33 or Yp11.32p11.31 (310,932-2,646,815 or 260,932-2,596,815) ×1, Yp11.2q12 (8,641,183-59,335,913) ×2. We conclude that the haploinsufficience of SHOX may be the cause of short stature and skeletal defects in the patient, while the non-obstructive azoospermia could be related to the lack of X-Y pairing during meiosis originated by the anomalous configuration of this chromosome abnormality and large deletion which occurred in Yp-PAR1.

摘要

Yq臂(以及AZF)的重复似乎可被具有生育能力的男性所耐受,而SHOX的突变、缺失、重复或单倍剂量不足可引发一系列广泛的表型,包括身材矮小和骨骼异常。我们报告了一例年轻男性的非梗阻性无精子症病例,该男性身材矮小、有骨骼异常、智力正常且激素参数正常。该男性表现出一种非常独特的Y染色体畸变,由Yq和Yp近端区域的重复以及Yptel中几乎所有PAR1的缺失组成,包括SHOX。使用了CBA和RBA显带以及用端粒、着丝粒、AZF和SHOX探针进行的FISH定位。这些结果通过阵列比较基因组杂交得到证实,其揭示了以下核型组成:arr [hg19] Xp22.33或Yp11.32p11.31(310,932 - 2,646,815或260,932 - 2,596,815)×1,Yp11.2q12(8,641,183 - 59,335,913)×2。我们得出结论,SHOX的单倍剂量不足可能是患者身材矮小和骨骼缺陷的原因,而非梗阻性无精子症可能与减数分裂期间X - Y配对缺乏有关,这是由该染色体异常的异常构型以及Yp - PAR1中发生的大片段缺失所导致的。

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