POMT2-related limb-girdle muscular dystrophy is a rare, inherited muscle disease. It weakens the muscles around the hips and shoulders first (the “limb-girdle” areas). The condition happens when a ...
Autosomal-recessive limb-girdle muscular dystrophy caused by mutation in the FKTN gene is a genetic muscle disease. It weakens the muscles around the hips and shoulders. It usually starts in ...
Autosomal recessive limb-girdle muscular dystrophy type 2M (LGMD2M) is a rare, inherited muscle disease caused by mutations in the FKTN gene (fukutin). Fukutin helps add sugar chains to a ...
Autosomal recessive limb-girdle muscular dystrophy caused by ANO5 mutation is a genetic muscle disease. It happens when a person inherits two faulty copies of the ANO5 gene (one from each parent). ...
Autosomal recessive limb-girdle muscular dystrophy type 2L (LGMD2L) is a genetic muscle disease that mainly weakens the muscles around the hips and shoulders (the “limb-girdle” muscles). It happens ...
Autosomal-Recessive Limb-Girdle Muscular Dystrophy Caused by Mutation in POMT1 is a genetic muscle disease. It weakens the muscles around the hips and shoulders (the “limb-girdle” muscles). It starts ...
Autosomal recessive limb-girdle muscular dystrophy type 2J (LGMD2J) is a genetic muscle-wasting disease caused by mutations in the TTN gene, which makes titin, a giant protein that works like a ...
FKRP-related limb-girdle muscular dystrophy is a genetic muscle disease. A person inherits two faulty copies of the FKRP gene. Because of this, a protein called fukutin-related protein does not work ...
Autosomal-recessive limb-girdle muscular dystrophy caused by FKRP mutations is a genetic muscle disease. It weakens the muscles around the hips, thighs, shoulders, and upper arms (the “limb ...
Autosomal recessive limb-girdle muscular dystrophy type 2I is a genetic muscle disease. It mainly weakens the muscles around the hips and shoulders. These are called the “limb-girdle” muscles. The ...
TRIM32-related limb-girdle muscular dystrophy R8 (LGMDR8) is a rare, inherited muscle disease. It mainly weakens the large muscles around the hips and shoulders (the “limb-girdle” muscles). It ...
TRIM32 autosomal-recessive limb-girdle muscular dystrophy is a rare genetic muscle disease in which both copies of a person’s TRIM32 gene carry harmful changes (variants). The TRIM32 gene makes a ...
Limb-girdle muscular dystrophy due to TRIM32 deficiency (LGMDR8) is a rare, inherited muscle disease. It mainly weakens the muscles around the hips and shoulders—the “limb girdles.” The problem comes ...
TRIM32-related limb-girdle muscular dystrophy is a rare, inherited muscle disease. It mainly weakens the limb-girdle muscles—the muscles around your hips and shoulders. Weakness grows slowly over ...
Autosomal recessive limb-girdle muscular dystrophy type 2H (LGMD2H) is a rare, inherited muscle disease caused by biallelic (two-copy) variants in the TRIM32 gene. It usually starts in late teens or ...
Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2G (LGMD2G) is a rare, inherited muscle disease. It weakens the muscles around the hips and shoulders (the “limb-girdle” area) and can also ...
Autosomal Recessive Limb-Girdle Muscular Dystrophy Caused by Mutation in the SGCD Gene is a rare inherited muscle disease. It slowly damages the muscles around the hips and shoulders (the ...
Autosomal recessive limb-girdle muscular dystrophy type 2F (LGMD2F) / LGMDR6 is a rare, inherited muscle disease that mainly weakens the muscles of the hips/thighs (pelvic girdle) and shoulders/upper ...
Autosomal-Recessive Limb-Girdle Muscular Dystrophy Caused by Mutation in SGCB is a genetic muscle disease. It happens when both copies of the SGCB gene (one from each parent) carry a harmful change. ...
Autosomal recessive limb-girdle muscular dystrophy due to SGCA is a genetic disease that weakens the muscles closest to the center of the body—especially the hips, thighs, shoulders, and upper arms. ...
