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Qualitative or quantitative defects of alpha-sarcoglycan

MONDO:0016141

Also known as: alpha-sarcoglycanopathy

3 clinical trials for this condition and its sub-types.

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Sub-types

Autosomal recessive limb-girdle muscular dystrophy type 2D (3)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Human disease (14) Hereditary neurological disease (5) Sarcoglycanopathy (3) Disease of genetic or genomic mechanism (2) Disease by body system or component (0) Disease by etiologic mechanism (0) Qualitative or quantitative protein defects in neuromuscular diseases (0)
Trials to join now! 1 Not yet finished but already full! 1 Terminated 1
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  • Scientists watch LGMD progress in 205 patients over years

    Knowledge-focused Ongoing

    This study follows 205 people with four types of limb-girdle muscular dystrophy (LGMD) to understand how the disease changes over time. Participants will have their muscle strength, movement, and breathing tested regularly for up to 5 years. No treatment is given; the goal is to …

    Sponsor: Sarepta Therapeutics, Inc. • Aim: Knowledge-focused

    Last updated Jun 27, 2026 07:56 UTC

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