Department of Genetics at Reproductive Biomedicine Research Center, Royan Institute for Reproductive biomedicine, ACECR, Tehran, Iran.
Gynecol Endocrinol. 2013 Jun;29(6):588-91. doi: 10.3109/09513590.2013.788625.
The importance of chromosomal abnormalities in etiology of premature ovarian failure (POF) is well known but in many cases, POF still remains idiopathic. We investigated the frequency and type of chromosomal aberrations in Iranian women diagnosed with idiopathic POF. Standard cytogenetic analysis was carried out in a total of 179 patients. Karyotype analysis of these patients revealed that 161 (89.95%) patients had normal female karyotype and 18 (10.05%) patients had abnormal karyotypes. The abnormal karyotypes included sex reverse sex determining region Y (SRY) negative (five Cases), X chromosome mosaicism (five cases), abnormal X chromosomes (three cases), abnormal autosomes (three cases) and X-autosome translocation (two cases). The overall prevalence of chromosomal abnormalities was 10.05% in this first large-scale report of chromosomal aberrations in Iranian women with POF. The results confirm previous observations and emphasis on the critical role of X chromosome abnormalities as one of the possible etiologies for POF.
染色体异常在卵巢早衰(POF)病因中的重要性是众所周知的,但在许多情况下,POF 仍然是特发性的。我们调查了伊朗特发性 POF 女性患者的染色体异常频率和类型。对 179 名患者进行了标准细胞遗传学分析。这些患者的核型分析显示,161 名(89.95%)患者具有正常女性核型,18 名(10.05%)患者具有异常核型。异常核型包括性反转性决定区 Y(SRY)阴性(5 例)、X 染色体镶嵌(5 例)、异常 X 染色体(3 例)、异常常染色体(3 例)和 X-常染色体易位(2 例)。在这项对伊朗 POF 女性染色体异常的首次大规模报告中,染色体异常的总体患病率为 10.05%。结果证实了先前的观察结果,并强调了 X 染色体异常作为 POF 可能病因之一的关键作用。