Gilgenkrantz S, Dulucq P, Bresson J L, Gouget A, Pernot C, Gregoire M J
J Med Genet. 1981 Dec;18(6):465-9. doi: 10.1136/jmg.18.6.465.
Five members of our study family were carriers of a balanced insertion (10;5) (q22;q13;q22). One of the children had psychomotor retardation and malformations resulting from a partial trisomy of the proximal long arm of chromosome 5, having received the maternal der(10). Amniocentesis identified another case of partial proximal trisomy in a fetus of a subsequent pregnancy. This clinical and family study is compared with two other published cases of proximal trisomy 5q.
我们研究的这个家族中有5名成员是平衡插入(10;5)(q22;q13;q22)的携带者。其中一个孩子患有精神运动发育迟缓以及因5号染色体长臂近端部分三体性导致的畸形,这是因为他遗传了母亲的der(10)。羊水穿刺检查在随后一次怀孕的胎儿中又发现了一例近端部分三体性的病例。本临床及家族研究与另外两篇已发表的5q近端三体性病例进行了比较。