Clin2
NCT00272883Possibly a fitRecruiting

Study genes in congenital muscle weakness

Central Core DiseaseCentronuclear MyopathyCongenital Fiber Type DisproportionMultiminicore DiseaseMyotubular MyopathyNemaline MyopathyRigid Spine Muscular DystrophyUndefined Congenital Myopathy

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital clinical trials.

This research study looks at genes and molecules to better understand congenital myopathies (birth-related muscle weakness). It may help explain the cause of symptoms and improve future diagnoses for you and your family.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
4,000 people
Ages
Any age
Study type
Observational

Who can take part

  • You have a clinical diagnosis or a suspected diagnosis of congenital myopathy
  • If you’re able, a family member is also willing to take part in the study
  • You should not have myotonia congenita or a related condition

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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