Thrilled to share my publication in Nature Magazine Genetics #WorldView section about #rarediseases and challanges we face in resource-likited country. Global collaboration is needed to diagnose, treat and councel all #undiagnosed children and their families! Prof Dr Arndt Rolfs , Reza Maroofian, Sofia Douzgou Houge Siddharth Banka Fowzan Alkuraya Joseph Gleeson Cederroth Helene Mikk Cederroth Peter Krawitz Behnam Javanmardi, PhD #GestaltMatcher #deeplasia #face2gene #FDNA Allan Bayat Stefan Barakat Shahida Moosa Gunnar Douzgos Houge Wilhelm Foundation UDNI Tbilisi State Medical University Ari ZIMRAN Elene Abzianidze Eka Kvaratskhelia ESHG European Society of Human Genetics ERN ITHACA
Thank you, Tika! We are so happy you like Wilhelm Foundation's efforts
Completely agree. But it is important that genetic testing will result in actionable treatment opportunities for many patients in these developing countries as well as an help for the families in reproductive-decision making to prevent the recurrent risk of the diseases.
Completely agree. We need collaborative efforts to find a solution for rare diseases. Let’s share our resources and concentrate our energy.
Thanks Tinatin Complete agree
Banoon ART and Cytogenetics Centre, Bahrain Defence Force Hospital
2wTrue, genomic testing is not affordable for many families with rare disease, especially in developing countries, collaboration is crucial. A nice article, thanks Tinatin.