Know LGMD
Limb-girdle muscular dystrophy (LGMD) is a group of genetic neuromuscular disorders that cause progressive muscle weakness, predominantly affecting the upper arms and legs ("limb") and the thoracic ("girdle") muscles.1,2
LGMD slows life down
LGMD is caused by mutations in genes responsible for proteins involved in muscle function and repair. LGMD2I/R9 (FKRP-related) is a form of LGMD caused by mutations in the FKRP gene.1,2
LGMD2I/R9 is commonly missed
Misdiagnosis or delays in diagnosis or receiving qualified medical attention are common with LGMD2I/R9 and can have a lasting impact.3 Learn about recognizing the early signs and confirming the diagnosis with genetic testing.
The current standard of care is limited, but essential
There are no approved therapies for LGMD2I/R9, and current treatment is limited to supportive care.3