Department of Genetic Medicine, Royal Manchester Children's Hospital, Manchester, UK.
J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S123-7. doi: 10.1007/s10545-009-9035-4. Epub 2010 Feb 18.
This article documents both the neurological and physical outcomes of the first published set of siblings undergoing transplantation at differing ages for α-mannosidosis. The older brother, the index case, was diagnosed at the age of 3 years and underwent transplantation at 13 years for the treatment of increasing somatic problems and recurrent infections. The younger brother had undergone transplantation pre-symptomatically at 6 months of age. Their clinical, radiological and developmental outcomes are documented and compared with the previous published cases, with the case for early transplantation being weighted against other potential therapies.
本文记录了第一组接受 α-甘露糖苷贮积症不同年龄移植的兄弟姐妹的神经和身体结果。哥哥是索引病例,3 岁时被诊断出来,13 岁时因躯体问题不断增加和反复感染接受了移植治疗。弟弟在 6 个月大时进行了症状前移植。本文记录并比较了他们的临床、影像学和发育结果,并与之前发表的病例进行了比较,认为早期移植的理由是对抗其他潜在疗法。