How many patients are there in Europe?

There is no complete European count. Patient registries (official databases that collect information about people with a specific disease to support research and care) and international collaboration are essential to building a clearer picture. Enrolling in a patient registry directly supports research and improved healthcare for everyone with LAMA2-RD. contact us and we can help direct you.

What is LAMA2-RD? What does LAMA2 stand for? What causes LAMA2-RD? What is the role of the LAMA2 gene? What does the laminin alpha-2 protein do in the body? What is the difference between LAMA2-RD, MDC1A, merosin-deficient congenital muscular dystrophy and LAMA2-CMD? Is LAMA2-RD a muscle disease? How rare is LAMA2-RD? How many people worldwide are living with LAMA2-RD? How many LAMA2-RD patients are there in my country? What forms of LAMA2-RD exist? What is the difference between the severe and milder forms of LAMA2-RD? Is LAMA2-RD inherited? Can two healthy parents have a child with LAMA2-RD? What is the chance that another child in our family will have LAMA2-RD? Is prenatal testing available for LAMA2-RD? Is preimplantation genetic testing possible? What is the difference between the LAMA2 gene and the laminin alpha-2 protein

How many patients are there in Europe?

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