Linden M G, Bender B G, Robinson A
Department of Pediatrics, National Jewish Center for Immunology and Respiratory Medicine, Denver, CO 80206, USA.
Pediatrics. 1995 Oct;96(4 Pt 1):672-82.
Sex chromosome abnormalities occur in at least 1 in 400 births and include the well-described 47,XXX, 47,XXY, 47,XYY, and 45,X karyotypes. The addition of more than one extra X or Y chromosome occurs rarely, and little information is available in the medical literature. Individual case reports make up most of this body of knowledge, and all are based on subjects who identified themselves postnatally. Many were ascertained through screenings of institutions and hospitals; thus, there is no unbiased information on the natural history of poly X and Y karyotypes. A direct relationship between the number of additional sex chromosomes and the severity of the phenotype is generally assumed. The purpose of this article is to summarize what is known about these conditions and to present 10 additional cases. The karyotypes include, 48,XXXX, 49,XXXXX, 48,XXYY, 48,XXXY, 49,XXXXY, 49,XXXYY, 48,XYYY, 49,XYYYY, and 49,XXYYY.
性染色体异常在至少每400例出生中就有1例发生,包括常见的47,XXX、47,XXY、47,XYY和45,X核型。额外增加一条以上X或Y染色体的情况很少见,医学文献中相关信息也很少。这方面的知识大多是个别病例报告,且均基于出生后自我认定的个体。许多病例是通过机构和医院筛查确定的;因此,关于多X和Y核型的自然病史没有无偏倚的信息。一般认为额外性染色体的数量与表型严重程度之间存在直接关系。本文的目的是总结关于这些情况的已知信息,并呈现另外10例病例。核型包括48,XXXX、49,XXXXX、48,XXYY、48,XXXY、49,XXXXY、49,XXXYY、48,XYYY、49,XYYYY和49,XXYYY。