Sarcoglycanopathy
MONDO:0016140Deficiencies or mutations in the genes for the sarcoglycan complex subunits. A variety of phenotypes are associated with these mutations including a subgroup of autosomal recessive limb girdle muscular dystrophies, cardiomyopathies, and respiratory deficiency.
Also known as: qualitative or quantitative defects of sarcoglycan
9 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Autosomal recessive limb-girdle muscular dystrophy type 2E
(5)
Autosomal recessive limb-girdle muscular dystrophy type 2C
(4)
Autosomal recessive limb-girdle muscular dystrophy type 2D
(3)
Autosomal recessive limb-girdle muscular dystrophy type 2F
(1)
Qualitative or quantitative defects of gamma-sarcoglycan
(1)
Dilated cardiomyopathy 1L
(0)
Qualitative or quantitative defects of alpha-sarcoglycan
(0)
Qualitative or quantitative defects of beta-sarcoglycan
(0)
Qualitative or quantitative defects of delta-sarcoglycan
(0)