Fryns J P, Detavernier F, van Fleteren A, van den Berghe H
Hum Genet. 1978 Oct 31;44(2):201-5. doi: 10.1007/BF00295415.
This paper describes a case of partial trisomy of almost the entire long arm of chromosome 18 in a newborn with classic trisomy-18 phenotype, resulting from a de novo unbalanced 181/21p translocation: karyotype: 46,XX,-21,t(18;21)(18qter leads to 18q11 ::21p12 leads to 21qter). A review of the other reported cases of partial trisomy 18 suggests that a critical segment in chromosome 18, corresponding to bands q11-q12, might be responsible for most of the signs of trisomy 18, including failure to thrive and early death.
本文描述了一名患有典型18三体综合征表型的新生儿,其18号染色体长臂几乎全部部分三体,这是由新发的不平衡18;21p易位所致:核型为:46,XX,-21,t(18;21)(18qter导致18q11::21p12导致21qter)。对其他已报道的18号染色体部分三体病例的回顾表明,18号染色体上对应于q11-q12带的关键区段可能是导致18三体综合征的大多数体征的原因,包括生长发育迟缓及早期死亡。