How many LAMA2-RD patients are there in my country?

In many countries, exact numbers are still not known. This depends on your national neuromuscular registry and patient organizations. If you are not sure where to start, contact us and we can help direct you to your national organizations.

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 patients are there in Europe? 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

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