The Journal Rare Disorders: Diagnosis & Therapy is an open access Scientific Journal which mainly focuses on articles of rare and chronically debilitating diseases. The Journal Rare Disorders: Diagnosis & Therapy comes up with an opportunity to researchers and scientist to explore rare diseases and their therapies. The Journal Rare Disorders: Diagnosis & Therapy is of highest standards in terms of quality.

National Academies of Sciences, Engineering, and Medicine; Health and Medicine Division; Board on Health Sciences Policy; Roundtable on Genomics and Precision Health.National Academies (US); 2018 Mar 16.

A population-based registry as a source of health indicators for rare diseases: the ten-year experience of the Veneto Region’s rare diseases registry. Mazzucato M, Visonà Dalla Pozza L, Manea S, Minichiello C, Facchin P.

Tumori. 2012 Sep-Oct;98(5):550-8. doi: 10.1700/1190.13194. The burden of rare cancers in Italy: the surveillance of rare cancers in Italy (RITA) project. Mallone S, Ferretti S, Meduri F, Capocaccia R, Gatta G; RITA working group.

According to Eurodis News Agency:

Durhane Wong-Rig, Chair of the RDI Council, and Yann Le Cam, Chief Executive Officer of EURORDIS, sign the MoU

The vision of the Sustainable Development Goals is a world in which no one is left behind, including people who suffer from rare diseases. Just because a disease affects a small number of people does not make it irrelevant or less important than diseases that affect millions.

Rare Diseases Foundation of Iran attended the European Conference on Rare Diseases and Orphan Drugs and accepted to sign a document on Diagnosis and pharmaceutical collaboration with EURORDIS.

Open Call for NGOs to apply for Consultative Status with the United Nations (Deadline: 1 June 2018)

NGOs interested in applying for ECOSOC consultative status should submit their application and required documents on or before the deadline of 1 June 2018. The following link provides background information, the benefits of consultative status and instructions for how to apply: https://bit.ly/2ozYpVw  

The 2018 RDI General Assembly (open to RDI members only) and Annual Meeting (open to everyone interested in learning more about international rare disease initiatives) will also take place on 10 May in conjunction with ECRD.

Register to attend

On the occasion of Rare Disease Day

Rare Diseases Foundation of Iran held Genodermatoses symposium

The symposium of Rare Condition of Skin Disease (Genodermatoses) held by Rare Diseases Foundation of Iran in collaboration with Dermatology and Stem Cell Research Center and Tehran University of Medical Sciences on February, 26, 2018 in Tehran.