Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders
Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders
About this item
Full title
Author / Creator
Publisher
Cham: Springer International Publishing
Journal title
Language
English
Formats
Publication information
Publisher
Cham: Springer International Publishing
Subjects
More information
Scope and Contents
Contents
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 decreasin...
Alternative Titles
Full title
Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders
Authors, Artists and Contributors
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_proquest_miscellaneous_80179719
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_80179719
Other Identifiers
ISSN
1018-4813
E-ISSN
1476-5438
DOI
10.1038/sj.ejhg.5201135