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 ...
Dr. Reem Saadeh Haddad, MD - Clinical Genetics, Genomics, Cytogenetics, Biochemical Genetics Specialist
Autosomal recessive limb-girdle muscular dystrophy type 2E (LGMD2E), now called LGMDR4 (beta-sarcoglycan–related), is a rare genetic muscle disease. It weakens ...
Adhalinopathy is a rare inherited muscle disease caused by a lack or severe shortage of a protein called alpha-sarcoglycan (older name: adhalin). ...
Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency is a genetic muscle disease that mostly weakens the muscles around the hips and shoulders. ...
Sarcoglycanopathies are a group of inherited muscle diseases that mainly weaken the shoulder and hip muscles (the “limb-girdle” muscles). They happen when one ...
Duchenne-like autosomal recessive muscular dystrophy type 2 is a genetic muscle disorder. It weakens the muscles around the hips and shoulders first (the ...
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 ...
Alpha-sarcoglycanopathy is a rare, inherited muscle-wasting disease caused by biallelic (recessive) mutations in the SGCA gene, which encodes the α-sarcoglycan ...
Alpha-sarcoglycan–related limb-girdle muscular dystrophy R3 is a rare, inherited muscle disease caused by harmful changes (variants) in the SGCA gene. SGCA ...
Autosomal recessive limb-girdle muscular dystrophy type 2D is a genetic muscle disease. It happens when both copies of a gene called SGCA are changed ...
Severe childhood autosomal recessive muscular dystrophy, North African type, is a genetic muscle disease that usually starts in early childhood. It makes the ...
Maghrebian myopathy is an inherited muscle disease that weakens the muscles around the hips and shoulders (the “limb-girdle” muscles). Doctors also call it ...
Limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency is a rare, inherited muscle disease. It mainly weakens the muscles around the hips, thighs, ...
Gamma-sarcoglycanopathy is a genetic muscle disease caused by harmful changes (variants) in the SGCG gene. This gene helps make γ-sarcoglycan, one piece of a ...
Gamma-sarcoglycan-related limb-girdle muscular dystrophy R5 (LGMDR5) is a rare genetic muscle disease. It happens when both copies of a gene called SGCG do not ...
Autosomal recessive limb-girdle muscular dystrophy caused by SGCG mutation (γ-sarcoglycanopathy / LGMDR5) is a genetic muscle disorder. It happens when both ...
Autosomal recessive Duchenne-like muscular dystrophy type 1 is a rare genetic muscle disease caused by harmful changes (mutations) in the SGCG gene, which ...
Autosomal recessive limb-girdle muscular dystrophy type 2C (LGMD2C) is a genetic muscle disease that mainly weakens the muscles around the hips and shoulders ...
Limb-girdle muscular dystrophy type 3 (LGMDR3) is a rare, inherited muscle disease. It mainly weakens the muscles around the hips and shoulders (the “limb ...
Limb-Girdle Muscular Dystrophy due to Dysferlin Deficiency (LGMDR2) is a genetic muscle disease. “Genetic” means it is caused by changes (mutations) in a gene. ...
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