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Rare Disease Connection

If you or someone you love is affected by a rare disease, you likely have more questions than answers. That’s why we’re here. Rare Disease Connection, and our additional resources on RareDisease.com and YourDNA.com, brings together the people whose expertise can explain what you’re facing. From diagnosis, to prognosis, to treatment options, all the way to questions like “Who do I talk to? Where are the people who’ve been through this before?”. We have the answers, direct from the experts and those who've faced your disease.

info_outline TANGO2-related metabolic encephalopathy and arrhythmias 08/25/2020
info_outline Very long-chain acyl-CoA dehydrogenase (VLCAD) 08/18/2020
info_outline Duchenne Muscular Dystrophy 07/22/2020
info_outline Fragile X Syndrome 06/24/2020
info_outline Multiple Sulfatase Deficiency 07/06/2020
info_outline Charcot Marie Tooth (CMT) 06/03/2020
info_outline 22q Deletion Syndrome 05/30/2020
info_outline Huntington's Disease 05/01/2020
info_outline Ehlers-Danlos Syndrome (EDS) 04/01/2020
info_outline Lynch Syndrome 03/31/2020
info_outline Neurofibromatosis 03/31/2020
info_outline Trisomy 13 / Patau 02/27/2020
info_outline Klinefelter Syndrome 02/27/2020
info_outline Fabry Disease 02/27/2020
info_outline What is Rare Disease Connection? 02/27/2020
 
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