Vianna-Morgante A M, Nunesmaia H G
J Med Genet. 1978 Aug;15(4):305-10. doi: 10.1136/jmg.15.4.305.
A patient is described with some features of Down's syndrome and a 45,XY, t(15;21)(15qter leads to 15p13::21p11 leads to 21qter)/46,XY,i(21)(qter leads to cen leads to qter) karyotype. Two mechanisms are proposed for the origin of the mosaicism, one assuming the dissociation of a translocation (15;21) chromosome already present in the zygote, and the other involving a chromatid translocation in a 46,XY zygote. The possible independent origin of the two cell lines is also considered.
描述了一名具有唐氏综合征某些特征且核型为45,XY,t(15;21)(15qter导致15p13::21p11导致21qter)/46,XY,i(21)(qter导致cen导致qter)的患者。提出了两种嵌合体起源机制,一种假设合子中已存在的易位(15;21)染色体解离,另一种涉及46,XY合子中的染色单体易位。还考虑了两种细胞系可能的独立起源。