Understanding CRYAB Gene Myopathy Myofibrillar Fatal Infantile Hypertrophy Alpha-B Crystallin-Related Genetic Test Genetic advancements have paved the way for identifying and understanding rare genetic conditions that affect individuals right from infancy. One such condition is associated with mutations in the CRYAB gene, leading to a spectrum of myopathic disorders. Among these, Myofibrillar Myopathy (MFM) with […]
