Cowell H R, Clark C E
Clin Orthop Relat Res. 1978 Sep(135):4-14.
Patients with orthopedic problems may also have chromosomal abnormalities. Individuals who present with subtle clinical findings suggestive of a known syndrome resulting from a chromosomal abnormality, such as Klinefelter syndrome, Turner syndrome, or any of the known trisomiers, should be investigated further in order to confirm the diagnosis. In addition, those patients who have multiple congenital abnormalities in several systems should also have chromosome analysis. This should be done not only to gain new information in regard to chromosome abnormalities, but also to establish a diagnosis for the individual and thus provide proper genetic counseling for the family. If the clinical picture strongly suggests a chromosomal abnormality, and routine karyotyping does not demonstrate one, it is imperative that one or more banding techniques be utilized before a chromosomal abnormality can be ruled out.
患有骨科问题的患者也可能存在染色体异常。那些表现出细微临床症状、提示由染色体异常导致的已知综合征(如克兰费尔特综合征、特纳综合征或任何已知的三体综合征)的个体,应进一步进行检查以确诊。此外,那些在多个系统中存在多种先天性异常的患者也应进行染色体分析。这样做不仅是为了获取有关染色体异常的新信息,也是为了给个体确诊,从而为其家庭提供适当的遗传咨询。如果临床表现强烈提示染色体异常,而常规核型分析未显示异常,则必须在排除染色体异常之前采用一种或多种显带技术。