This week, Mystery Monday focussed on Congenital Muscular Dystrophy with thanks to Cure CMD for the fantastic resources. Congenital Muscular Dystrophy (CMD) is a rare and debilitating genetic disorder that […]
Have YOU heard of DHDDS-related conditions? This week Mystery Monday is focusing on the gene known as DHDDS and its role in cases of ataxia, cerebellar and neurodevelopmental conditions. Thank […]
This week Mystery Monday is focusing on Superficial Siderosis. Thank you so much to the Superficial Siderosis Research Alliance for the fantastic resources! Be sure to stay in the loop […]
This week Mystery Monday is focusing on Haemochromatosis? Thank you so much to Haemochromatosis UK for the fantastic resources! Be sure to stay in the loop with Mystery Monday by […]
This week Mystery Monday is focusing on CASK-Related Disorders? Thank you so much to CASK Research Foundation for the fantastic resources! Be sure to stay in the loop with Mystery […]
Who are Unique? In the world of rare genetic conditions, understanding the intricacies of a specific disorder and accessing comprehensive information can be a daunting task for families and healthcare […]
This week Mystery Monday is focusing on Barth syndrome! Thank you so much to Barth syndrome UK for the fantastic resources! Be sure to stay in the loop with Mystery […]
This week Mystery Monday is focusing on Osteogenesis Imperfecta! Thank you so much to Osteogenesis Imperfecta Federation Europe (OIFE) for the fantastic resources! Be sure to stay in the loop […]
Have YOU heard of Porphyria? This week Mystery Monday is focusing on Porphyria! Thank you so much to the British Porphyria Association for the fantastic resources! Be sure to stay […]
Mystery Monday is BACK and this week we are focusing on Familial Intracranial Aneurysms! Thank you so much to HBA Support for the fantastic resources! Be sure to stay in […]
