Barber J C, Temple I K, Campbell P L, Collinson M N, Campbell C M, Renshaw R M, Dennis N R
Wessex Regional Genetics Laboratory, Salisbury District Hospital, United Kingdom.
Am J Med Genet. 1996 Mar 1;62(1):84-90. doi: 10.1002/(SICI)1096-8628(19960301)62:1<84::AID-AJMG17>3.0.CO;2-R.
We present two families with different distal long arm 5;10 translocations. In one family the propositus and his mother inherited the same derived chromosome 10 from the maternal grandfather who has a balanced t(5;10)(q35.3;q26.13). The phenotype of both the affected patients is milder and only partially overlaps with that of previous cases of distal 10q deletion. Other previously reported cases of transmitted imbalance are also remarkable for mild phenotype, occurrence of deletions rather than duplications and a strong bias toward maternal as opposed to paternal transmission. In the second family, the propositus inherited a derived chromosome 10 from his mother who carries a balanced (t(5;10)(q35.1;q26.3) translocation; his clinical manifestations are consistent with an emerging phenotype for distal 5q duplications.
我们展示了两个具有不同5号和10号染色体长臂远端易位的家族。在一个家族中,先证者及其母亲从外祖父那里继承了相同的衍生10号染色体,外祖父携带平衡的t(5;10)(q35.3;q26.13)。两名受影响患者的表型较轻,仅部分与先前远端10q缺失病例的表型重叠。其他先前报道的传递不平衡病例也具有表型较轻、缺失而非重复的发生以及母系传递相对于父系传递的强烈偏向等特点。在第二个家族中,先证者从携带平衡(t(5;10)(q35.1;q26.3)易位的母亲那里继承了一条衍生10号染色体;他的临床表现与远端5q重复的新出现表型一致。