Abd S E, Wilson L, Howlin P, Patton M A, Wintgens A M, Wilson R
St George's Hospital Medical School, London, UK.
Dev Med Child Neurol. 1997 Feb;39(2):119-24. doi: 10.1111/j.1469-8749.1997.tb07394.x.
An 8-year-old girl with Turner syndrome and 45,X/46,X,r(X) mosaicism was found to have agenesis of the corpus callosum and various other characteristics including 'kabuki makeup' facial features and mild learning disability. Only two other cases of Turner syndrome associated with agenesis of the corpus callosum have been reported, both in patients with a 45,X karyotype. In both of those patients the constellation of signs differed from those of the present patient in a number of ways. It remains to be confirmed whether there is a higher incidence of CNS malformation in girls who have Turner syndrome with a ring X than has been reported for girls with Turner syndrome in general.
一名患有特纳综合征且核型为45,X/46,X,r(X)嵌合体的8岁女孩,被发现患有胼胝体发育不全以及其他各种特征,包括具有“歌舞伎妆容”的面部特征和轻度学习障碍。此前仅报道过另外两例与胼胝体发育不全相关的特纳综合征病例,这两名患者的核型均为45,X。在这两名患者中,体征组合在许多方面与当前患者不同。对于患有环形X染色体的特纳综合征女孩,其中枢神经系统畸形的发生率是否高于一般报道的特纳综合征女孩,仍有待证实。