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Selenoprotein N-related Myopathy
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Selenoprotein N-related Myopathy trials you may qualify forClinical trial pipeline · Data from ClinicalTrials.gov
See which Selenoprotein N-related Myopathy trials you may qualify forSELENON-related myopathy (SELENON-RM) and LAMA2-related muscular dystrophy (LAMA2-MD) are congenital neuromuscular disorders presenting with slowly, progressive…
The Congenital Muscle Disease Patient and Proxy Reported Outcome Study (CMDPROS) is a longitudinal 10 year study to identify and trend care parameters, adverse…
SEPN1 (SELENON) is a rare congenital myopathy due to mutations in the SELENON gene. MDC1A is a rare congenital muscle dystrophy due to mutations in the LAMA2 ge…
The objective of this study is to determine whether the administration of N-acetylcysteine (NAC) improves oxidative stress. To determine this, the study will as…