LAMA2-CMD · Merosin-deficient congenital muscular dystrophy · MDC1A · Kongenitale Muskeldystrophie Typ 1A · LAMA2-assoziierte Muskeldystrophie
This is an inherited muscle disorder caused by a deficiency of laminin-alpha-2, a vital protein that acts as a structural anchor to keep muscle fibers stable. Without this protein, the skeletal muscles progressively break down and weaken over time. This leads to a gradual loss of mobility and strength across the dog's entire muscular system.
Symptoms typically appear in early puppyhood, with owners noticing severe muscle weakness, stiffness, and difficulty walking. Over time, there is a visible loss of muscle mass as the condition progresses.
There is no cure for this condition, meaning treatment is lifelong and focused on supportive care, such as physical therapy, to maintain comfort. Managing this progressive disease typically costs between 1,500 and 6,000 EUR.
Estimated range of typical treatment cost. Actual cost depends on severity, clinic and region.
More conditions affecting the General / metabolic.