Building treasures for rare disorders

被引:12
|
作者
Baas, Melanie [1 ]
Huisman, Sylvia [1 ]
van Heukelingen, John [2 ]
Koekkoek, Gerritjan [3 ]
Laan, Henk-Willem [4 ]
Hennekam, Raoul C. [5 ]
机构
[1] Univ Amsterdam, AMC, Dept Paediat, NL-1012 WX Amsterdam, Netherlands
[2] Pitt Hopkins Parents Support Grp, Leidschendam, Netherlands
[3] Cornelia Lange Syndrome Support Grp, Ijmuiden, Netherlands
[4] Marshall Smith Syndrome Fdn, The Hague, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Paediat & Translat Genet, NL-1105 AZ Amsterdam, Netherlands
关键词
Internet; eHealth; Innovation; Wiki; Rare disorders; MARSHALL-SMITH SYNDROME;
D O I
10.1016/j.ejmg.2014.10.006
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The internet pre-eminently marks an era with unprecedented chances for patient care. Especially individuals with rare disorders and their families can benefit. Their handicap of low numbers vanishes and can become a strength, as small, motivated and well-organized international support groups allow easily fruitful collaborations with physicians and researchers. Jointly setting research agendas and building wikipedias has eventually led to building of multi-lingual databases of longitudinal data on physical and behavioural characteristics of individuals with several rare disorders which we call waihonapedias (waihona meaning treasure in Hawaiian). There are hurdles to take, like online security and reliability of diagnoses, but sharing experiences and true collaborations will allow better research and patient care for fewer costs to patients with rare disorders. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:11 / 13
页数:3
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