Kelly T E, Franko J B, Rogol A, Golden W L
Division of Medical Genetics, University of Virginia School of Medicine, Charlottesville, USA.
J Med Genet. 1998 Oct;35(10):862-4. doi: 10.1136/jmg.35.10.862.
Mosaicism introduces wide variability into the clinical expression of numerical and unbalanced structural chromosomal abnormalities. The phenotypic range of variability of 45,X/46,XY mosaicism extends from Turner syndrome to mixed gonadal dysgenesis to normal males. The specific phenotype is primarily dependent on the chromosomal constitution of the developing gonad. Similar phenotypic variability is observed with mosaicism for 45,X and a second cell line with an abnormal sex chromosome. This report describes a patient with Turner syndrome and a patient with mixed gonadal dysgenesis who have identical karyotypes, namely 45,X/46,X,idic(Y)(p11.2). While mosaicism alone might have accounted for the phenotypic differences, by PCR analysis the Turner syndrome patient was SRY and ZFY negative and the mixed gonadal dysgenesis patient was SRY and ZFY positive.
嵌合体使数目性和结构不平衡性染色体异常的临床表型呈现出广泛的变异性。45,X/46,XY嵌合体的表型变异范围从特纳综合征到混合型性腺发育不全,再到正常男性。具体的表型主要取决于发育中性腺的染色体组成。45,X与另一个具有异常性染色体的细胞系的嵌合体也观察到了类似的表型变异。本报告描述了一名患有特纳综合征的患者和一名患有混合型性腺发育不全的患者,他们具有相同的核型,即45,X/46,X,idic(Y)(p11.2)。虽然仅嵌合体本身可能解释了表型差异,但通过聚合酶链反应分析,特纳综合征患者的SRY和ZFY为阴性,而混合型性腺发育不全患者的SRY和ZFY为阳性。