Vogels Annick, Van Den Ende Jenneke, Keymolen Kathelijne, Mortier Geert, Devriendt Koen, Legius E, Fryns J P
Centre for Human Genetics, University of Leuven, Leuven, Belgium.
Eur J Hum Genet. 2004 Mar;12(3):238-40. doi: 10.1038/sj.ejhg.5201135.
The identification of all people with a diagnosis of Prader-Willi syndrome (PWS) confirmed by DNA methylation analysis living in Flanders was attempted through contact with the four genetic centres and the PWS Association. The birth incidence for the period 1993-2001 was 1:26 676, the minimum prevalence at 31 December 2001 was 1:76 574. A decreasing number of cases with age was found, which can be explained by a number of missing cases in the older population, a higher neonatal mortality in the past and an increasing mortality with age. Childhood death is usually sudden and associated with respiratory infection and high temperature, while the cause of death in adults is considered to be circulatory or respiratory in origin.
通过与四个基因中心和普拉德-威利综合征协会取得联系,尝试识别出居住在佛兰德地区、经DNA甲基化分析确诊患有普拉德-威利综合征(PWS)的所有人。1993年至2001年期间的出生发病率为1:26676,2001年12月31日的最低患病率为1:76574。发现病例数量随年龄增长而减少,这可以解释为老年人群中存在一些漏报病例、过去新生儿死亡率较高以及死亡率随年龄增长而上升。儿童期死亡通常较为突然,与呼吸道感染和高烧有关,而成年人的死因被认为源于循环系统或呼吸系统。