Gimelli G, Cinti R, Varone P, Naselli A, Di Battista E, Pezzolo A
Laboratorio di Citogenetica, Università di Genova, Italy.
Clin Genet. 1996 Jan;49(1):37-41. doi: 10.1111/j.1399-0004.1996.tb04322.x.
In this report, we describe a male infant with a 45,X karyotype; the entire short arm and the centromere of the Y chromosome were translocated onto the short arm of chromosome 18, resulting in an unbalanced dicentric chromosome. Breakpoints were identified by in situ fluorescence hybridization (FISH) on the proximal Yq11 and 18p11.2. Both Y and 18 centromeric alphoid sequences were identified on the derived 18 chromosome. Clinical features were compatible with 18p- syndrome and no Turner stigmata were present in our propositus. Short stature was likely to be related to the deletion of 18p and/or Yq, where a gene involved in stature determination has been located proximal to a gene involved in spermatogenesis (AZF).
在本报告中,我们描述了一名核型为45,X的男婴;Y染色体的整个短臂和着丝粒易位到18号染色体的短臂上,导致形成一条不平衡的双着丝粒染色体。通过对近端Yq11和18p11.2进行原位荧光杂交(FISH)确定了断点。在衍生的18号染色体上鉴定出了Y和18着丝粒α卫星序列。临床特征与18p-综合征相符,我们的先证者未出现特纳征。身材矮小可能与18p和/或Yq缺失有关,在Yq上靠近一个参与精子发生的基因(AZF)的位置有一个与身高决定有关的基因。