How rare is LAMA2-RD?

LAMA2-RD affects an estimated 1 to 4 people in every 100,000. It is the most common form of congenital muscular dystrophy (a muscle disease present from birth). Because it is rare and can be difficult to diagnose, the true number of people living with LAMA2-RD worldwide is probably higher than recorded.

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 many people worldwide are living with LAMA2-RD? How many patients are there in Europe? 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 rare is LAMA2-RD?

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