Bernardini Laura, Capalbo Anna, D'Avanzo Maria Gabriella, Torrente Isabella, Grammatico Paola, Dell'Edera Domenico, Cavalcanti Denise Pontes, Novelli Antonio, Dallapiccola Bruno
Ospedale Casa Sollievo della Sofferenza, San Giovanni Rotondo e Istituto CSS-Mendel, Roma, Italy.
Eur J Med Genet. 2007 Mar-Apr;50(2):94-102. doi: 10.1016/j.ejmg.2006.11.001. Epub 2006 Nov 23.
Genetic counselling of patients with small supernumerary ring chromosomes (sSRCs) can be difficult, especially in prenatal testing, due to the complexity in establishing a karyotype-phenotype correlation. In fact, it has been estimated that about 10% of extra ring(1) chromosomes are associated with an unremarkable phenotype. We report on five new cases of extra ring chromosomes(1) manifesting different clinical outcome. One case was familial, segregating from a mother with mosaic karyotype, while the others were de novo. Ring chromosomes were characterised by FISH. In three subjects the involvement of the same euchromatic 1p region was demonstrated. Present observations corroborate previous results and provide some insight into the identification of the harmless ring(1) structures.
对携带小的额外环状染色体(sSRCs)的患者进行遗传咨询可能会很困难,尤其是在产前检测中,因为建立核型与表型的相关性很复杂。事实上,据估计约10%的额外环状(1)染色体与不显著的表型相关。我们报告了5例额外环状(1)染色体表现出不同临床结果的新病例。1例为家族性,从具有嵌合核型的母亲遗传而来,其他病例为新发。通过荧光原位杂交(FISH)对环状染色体进行了特征分析。在3名受试者中证实了相同常染色质1p区域受累。目前的观察结果证实了先前的结果,并为识别无害的环状(1)结构提供了一些见解。