Requirements for a multicentric multidisciplinary registry on patients with disorders of sex development

Olaf Hiort, Lutz Wünsch, Martine Cools, Leendert Looijenga, Peter Cuckow

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

Samenvatting

Disorders of Sexual Development (DSDs) are a group of rare to very rare congenital anomalies of the genito-urinary tract of genetic and endocrine causes. Recently, an international database I-DSD was successfully implemented to register patients with DSD and to provide the basis for epidemiologic, genetic, and clinical research. This tool needs to be adjusted and supplemented with additional modules in order to better assess the anatomical basis of DSD as well as to monitor risk factors such as gonadal histology. A proposal for the additional information to be obtained is discussed.

Originele taal-2Engels
Pagina's (van-tot)624-8
Aantal pagina's5
TijdschriftJournal of pediatric urology
Volume8
Nummer van het tijdschrift6
DOI's
StatusGepubliceerd - dec. 2012
Extern gepubliceerdJa

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