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

被引：13
|
作者：
Hiort, Olaf [1 ]
Wuensch, Lutz [2 ]
Cools, Martine [3 ,4 ]
Looijenga, Leendert [5 ]
Cuckow, Peter [6 ]
机构：
[1] Univ Lubeck, Dept Paediat, Div Expt Paediat Endocrinol & Diabet, D-23560 Lubeck, Germany
[2] Univ Lubeck, Dept Paediat Surg, D-23560 Lubeck, Germany
[3] Ghent Univ Hosp, Dept Pediat Endocrinol, Ghent, Belgium
[4] Univ Ghent, B-9000 Ghent, Belgium
[5] Dr Daniel Den Hoed Canc Ctr, Dept Pathol, Erasmus Med Ctr, Josephine Nefkens Inst, NL-3008 AE Rotterdam, Netherlands
[6] Great Ormond St Hosp NHS Trust, Dept Urol, London, England
来源：
JOURNAL OF PEDIATRIC UROLOGY | 2012年 / 8卷 / 06期
关键词：
Sex development; MANAGEMENT; FEMALE; TUMORS; FORMS;
D O I：
10.1016/j.jpurol.2012.09.004
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
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. (C) 2012 Published by Elsevier Ltd on behalf of Journal of Pediatric Urology Company.
引用
收藏
页码：624 / 628
页数：5
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