Tiberio G
Centro Pediatrico Internazionale Luigi Gedda, Gregor Mendel Institute, Rome.
Acta Genet Med Gemellol (Roma). 1994;43(3-4):207-14. doi: 10.1017/s0001566000001963.
The 20 reported cases of MZ female twins discordant for X-linked diseases are reviewed. In such twins the X-inactivation pattern is opposite skewing (abnormal allele inactivated in most cells of the normal twin, and normal allele inactivated in most cells of the affected twin) or skewing in one twin and random in the cotwin. The diseases involved map in two specific regions: Xq27-28 and Xp21. The only exceptions are Fabry's disease and Aicardi's syndrome, which map in Xq22 and Xp22 respectively. No concordant MZ female carrier twins, either normal or affected, have been described. Three main hypotheses have been proposed to explain such characteristics [2, 5, 14], but none is completely satisfactory. The constant discordance for X-linked diseases in MZ female twins has important consequences for genetic counselling.
本文回顾了20例患X连锁疾病的单卵双生(MZ)女性双胞胎病例。在这类双胞胎中,X染色体失活模式为反向偏斜(正常双胞胎的大多数细胞中失活的是异常等位基因,而患病双胞胎的大多数细胞中失活的是正常等位基因),或者其中一个双胞胎存在偏斜,而其孪生同胞则是随机失活。所涉及的疾病定位于两个特定区域:Xq27 - 28和Xp21。仅有的例外是法布里病和艾卡迪综合征,它们分别定位于Xq22和Xp22。尚未有关于正常或患病的一致的MZ女性携带者双胞胎的描述。已提出三种主要假说来解释这些特征[2, 5, 14],但无一完全令人满意。MZ女性双胞胎中X连锁疾病的持续不一致性对遗传咨询具有重要意义。