Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders

157Citations
Citations of this article
62Readers
Mendeley users who have this article in their library.

Abstract

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. © 2004 Nature Publishing Group All rights reserved.

Cite

CITATION STYLE

APA

Vogels, A., Vand Den Ende, J., Keymolen, K., Mortier, G., Devriendt, K., Legius, E., & Fryns, J. P. (2004). Minimum prevalence, birth incidence and cause of death for Prader-Willi syndrome in Flanders. European Journal of Human Genetics, 12(3), 238–240. https://doi.org/10.1038/sj.ejhg.5201135

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free