FISH and PCR analyses in three patients with 45,X/46,X,idic(Y) karyotype: clinical and pathologic spectrum

Francisco Álvarez-Nava, Marisol Soto, María C Martínez, Minolfa Prieto, Zunilde Álvarez
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引用次数: 31

Abstract

Objective. – To delineate the phenotypic spectrum (clinical and gonadal features) from patients with a 45,X/46,X,mar(Y) karyotype based upon of their clinical, histological, cytogenetic and molecular evaluation.

Subjects. – Three patients with a 45,X/46,X,mar(Y) karyotype.

Methods. – Clinical assessment, karyotyping, endocrine evaluation, FISH and PCR analyses of several Y-chromosome loci and direct sequencing of the SRY gene.

Results. – The patients, two males and one female had varying degrees of impairment of sexual differentiation, with or without testis formation. One patient (reared as female and aged 17 years) had Turner syndrome with bilateral streak gonads. The second patient (2.4 years old) had ambiguous genitalia and presented a dysgenetic testis with a contralateral streak gonad. A third patient (26 years old) had bilateral dysgenetic testes (dysgenetic male pseudohermaphroditism). The ratio of 45,X vs. 46,X,+mar(Y) cells differed between patients and between different tissues. In each case the marker sexual chromosome was identified as a rearranged Y-chromosome (idic(Y)) using FISH and PCR analyses. In all cases the SRY gene was present in all tissues studied. No mutations were identified in this gene in any of the patients.

Conclusions. – The extent of male or female differentiation in these patients depends in part on the prevalence, time occurrence, and distribution of the 45,X cell line.

45、X/46、X、idic(Y)核型3例的FISH和PCR分析:临床和病理谱
目标。-根据临床、组织学、细胞遗传学和分子评价,描述45、X/46、X、mar(Y)核型患者的表型谱(临床和性腺特征)。- 3例核型分别为45、X/46、X、mar(Y)的患者。-临床评估、核型、内分泌评估、多个y染色体位点的FISH和PCR分析以及SRY基因的直接测序。-两男一女均有不同程度的性别分化障碍,有或无睾丸形成。1例患者(17岁女性)患有双侧性腺条纹的特纳综合征。第二例患者(2.4岁)生殖器模糊,表现为睾丸发育不良,对侧性腺条纹。第三例患者(26岁)双侧睾丸发育不良(男性假两性发育不良)。45、X和46、X、+mar(Y)细胞的比例在不同患者和不同组织之间存在差异。在每个病例中,标记性染色体被鉴定为重排的Y染色体(idic(Y)),使用FISH和PCR分析。在所有病例中,SRY基因都存在于所有研究的组织中。在所有患者中均未发现该基因突变。这些患者的男性或女性分化程度部分取决于45x细胞系的流行程度、发生时间和分布。
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