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Today on #RareDiseaseDay, we recognize the millions of individuals and families impacted by rare diseases —including our colleague Colin Sanford, whose daughter has a condition caused by a rare mutation in the KCNQ2 gene. KCNQ2-related disorders range from severe early-onset epilepsies, known as developmental and epileptic encephalopathies (DEEs), to milder forms referred to as self-limited (benign) neonatal epilepsies. These conditions can profoundly affect patients and their families, making research and awareness critical. Colin not only brings his expertise to Bioscribe but also serves as a board member of the KCNQ2 Cure Alliance, helping drive research, new therapy development, and advocacy for families navigating these challenges. At Bioscribe, we are proud to support life sciences companies working to better understand rare diseases and develop treatments that can change lives. Today, we stand with the entire rare disease community in the fight for greater awareness, research, and cures! #RareDiseaseDay2025 #StandUpForScience