Leeds Regional Cystic Fibrosis Centre, St James's University Hospital, Leeds, LS9 7TF, UK.
J Cyst Fibros. 2010 Sep;9(5):330-1. doi: 10.1016/j.jcf.2010.05.003. Epub 2010 Jun 11.
Previous reports of children with co-existence of cystic fibrosis and full trisomy 21 suggest a very poor prognosis, with the majority of cases dying in infancy and the oldest reported survivor being 6 years of age. We report the case of a young man with genetically confirmed trisomy 21 and homozygous for the F508del cystic fibrosis mutation. Despite the diagnosis of cystic fibrosis being delayed until the age of 2 years he has transitioned to adult services and is now 25 years of age. Currently he has poor lung function and a continuous ambulatory oxygen requirement.
先前有报道称囊性纤维化和完全 21 三体综合征共存的儿童预后极差,大多数病例在婴儿期死亡,有记录的存活时间最长的患儿为 6 岁。我们报告了一例经基因确诊的 21 三体综合征患者,且纯合子携带 F508del 囊性纤维化突变。尽管囊性纤维化的诊断被延迟到 2 岁,但他已过渡到成人服务,现在已经 25 岁了。目前,他的肺功能较差,需要持续的门诊吸氧。