Transcriptomic Analysis to Put an End to Misdiagnosis in Patients With Rare Muscle Diseases
Transcriptomic Analysis to Put an End to Misdiagnosis in Patients With Rare Muscle Diseases
Recruiting · NCT06833489 · Registry updated 2025-02-18Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Transcriptomic Analysis to Put an End to Misdiagnosis in Patients With Rare Muscle Diseases | Becker muscular dystrophy, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Duchenne muscular dystrophy, Lysosomal Storage Diseases, Nervous System, Muscular Disorders, Atrophic, Nutritional and Metabolic Diseases, Thomsen and Becker disease, X-linked disease, brain disorder, central nervous system disorder, congenital myopathy, disorder of glycogen metabolism, glycogen storage disease II, hereditary disease, inborn carbohydrate metabolic disorder, inborn errors of metabolism, inherited neurodegenerative disorder, lysosomal storage disease, metabolic disease, muscle tissue disorder, muscular dystrophy, musculoskeletal system disorder, myotonic syndrome, nervous system disorder, neurodegenerative disease, neuromuscular disease | Recruiting | Not applicable | 2025-02-18 | NCT06833489 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Assistance Publique Hopitaux De Marseille | 131 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Hopital Timone | Marseille | France | 1 |