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The need for worldwide policy and action plans for rare diseases
There are more than 6000 rare diseases (defined as affecting <5/10 000 individuals in Europe, <200 000 people in the United States). The rarity can create problems including: difficulties in obtaining timely, accurate diagnoses; lack of experienced healthcare providers; useful, reliable and ti...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443385/ https://www.ncbi.nlm.nih.gov/pubmed/22519914 http://dx.doi.org/10.1111/j.1651-2227.2012.02705.x |
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author | Forman, John Taruscio, Domenica Llera, Virginia A Barrera, Luis A Coté, Timothy R Edfjäll, Catarina Gavhed, Désirée Haffner, Marlene E Nishimura, Yukiko Posada, Manuel Tambuyzer, Erik Groft, Stephen C Henter, Jan-Inge |
author_facet | Forman, John Taruscio, Domenica Llera, Virginia A Barrera, Luis A Coté, Timothy R Edfjäll, Catarina Gavhed, Désirée Haffner, Marlene E Nishimura, Yukiko Posada, Manuel Tambuyzer, Erik Groft, Stephen C Henter, Jan-Inge |
author_sort | Forman, John |
collection | PubMed |
description | There are more than 6000 rare diseases (defined as affecting <5/10 000 individuals in Europe, <200 000 people in the United States). The rarity can create problems including: difficulties in obtaining timely, accurate diagnoses; lack of experienced healthcare providers; useful, reliable and timely information may be hard to find; research activities are less common; developing new medicines may not be economically feasible; treatments are sometimes very expensive; and in developing countries, the problems are compounded by other resource limitations. Emphasis is required to support appropriate research and development leading to better prevention, diagnosis and treatments of rare diseases. Notably, clinical trials using already existing drugs may result in new, affordable, treatment strategies. Moreover, rare diseases may teach us about common disorders. CONCLUSIONS: Countries are encouraged to implement specific research and development activities within their individual capabilities, so that patients worldwide have equal access to necessary interventions to maximize the potential of every individual. |
format | Online Article Text |
id | pubmed-3443385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-34433852012-09-17 The need for worldwide policy and action plans for rare diseases Forman, John Taruscio, Domenica Llera, Virginia A Barrera, Luis A Coté, Timothy R Edfjäll, Catarina Gavhed, Désirée Haffner, Marlene E Nishimura, Yukiko Posada, Manuel Tambuyzer, Erik Groft, Stephen C Henter, Jan-Inge Acta Paediatr Viewpoint Article There are more than 6000 rare diseases (defined as affecting <5/10 000 individuals in Europe, <200 000 people in the United States). The rarity can create problems including: difficulties in obtaining timely, accurate diagnoses; lack of experienced healthcare providers; useful, reliable and timely information may be hard to find; research activities are less common; developing new medicines may not be economically feasible; treatments are sometimes very expensive; and in developing countries, the problems are compounded by other resource limitations. Emphasis is required to support appropriate research and development leading to better prevention, diagnosis and treatments of rare diseases. Notably, clinical trials using already existing drugs may result in new, affordable, treatment strategies. Moreover, rare diseases may teach us about common disorders. CONCLUSIONS: Countries are encouraged to implement specific research and development activities within their individual capabilities, so that patients worldwide have equal access to necessary interventions to maximize the potential of every individual. Blackwell Publishing Ltd 2012-08 /pmc/articles/PMC3443385/ /pubmed/22519914 http://dx.doi.org/10.1111/j.1651-2227.2012.02705.x Text en © 2012 The Author(s)/Acta Pædiatrica © 2012 Foundation Acta Pædiatrica http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Viewpoint Article Forman, John Taruscio, Domenica Llera, Virginia A Barrera, Luis A Coté, Timothy R Edfjäll, Catarina Gavhed, Désirée Haffner, Marlene E Nishimura, Yukiko Posada, Manuel Tambuyzer, Erik Groft, Stephen C Henter, Jan-Inge The need for worldwide policy and action plans for rare diseases |
title | The need for worldwide policy and action plans for rare diseases |
title_full | The need for worldwide policy and action plans for rare diseases |
title_fullStr | The need for worldwide policy and action plans for rare diseases |
title_full_unstemmed | The need for worldwide policy and action plans for rare diseases |
title_short | The need for worldwide policy and action plans for rare diseases |
title_sort | need for worldwide policy and action plans for rare diseases |
topic | Viewpoint Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3443385/ https://www.ncbi.nlm.nih.gov/pubmed/22519914 http://dx.doi.org/10.1111/j.1651-2227.2012.02705.x |
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