Carakushansky G, Teich E, Ribeiro M G, Horowitz D D, Pellegrini S
Department of Pediatrics, School of Medicine, Federal University of Rio de Janeiro, Brazil.
Am J Med Genet. 1994 Oct 1;52(4):399-401. doi: 10.1002/ajmg.1320520402.
Here we report on a girl with diploid/triploid mosaicism followed up to age 5 years. The clinical manifestations are compared to those of other reported cases. In contrast to most cases, our patient was not growth retarded despite severe delays in psychomotor development. We also discuss 2 manifestations that have not received sufficient attention in previous reports: pigmentary dysplasia and truncal obesity.
在此,我们报告一名患有二倍体/三倍体嵌合体的女童,随访至5岁。将其临床表现与其他已报道病例的表现进行了比较。与大多数病例不同的是,尽管我们的患者精神运动发育严重迟缓,但并未出现生长发育迟缓。我们还讨论了两个在以往报告中未得到充分关注的表现:色素发育异常和躯干肥胖。