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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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_80179719

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

About this item

Full title

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

Publisher

Cham: Springer International Publishing

Journal title

European journal of human genetics : EJHG, 2004-03, Vol.12 (3), p.238-240

Language

English

Formats

Publication information

Publisher

Cham: Springer International Publishing

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

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

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