The need for worldwide policy and action plans for rare diseases

Abstract

UNLABELLED 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.

DOI: 10.1111/j.1651-2227.2012.02705.x

Extracted Key Phrases

1 Figure or Table

020406020132014201520162017
Citations per Year

79 Citations

Semantic Scholar estimates that this publication has 79 citations based on the available data.

See our FAQ for additional information.

Cite this paper

@inproceedings{Forman2012TheNF, title={The need for worldwide policy and action plans for rare diseases}, author={John P . Forman and Domenica Taruscio and Virginia A Llera and L. A. Barrera and Timothy R. Cot{\'e} and Catarina Edfj{\"a}ll and D{\'e}s{\'i}r{\'e}e C. E. Gavhed and Marlene E. Haffner and Yukiko Nishimura and Manuel Posada and Erik T Tambuyzer and Stephen C Groft and J Inge Henter}, booktitle={Acta paediatrica}, year={2012} }