questionsmedicales.fr
Maladies du système nerveux
Maladies neuromusculaires
Maladies musculaires
Maladies musculaires : Questions médicales fréquentes
Diagnostic
5
Maladies musculaires
Électromyographie
Force musculaire
Évaluation fonctionnelle
Biopsie musculaire
Myopathies
Créatine kinase
Maladies musculaires
Tests génétiques
Maladies musculaires héréditaires
Symptômes
5
Symptômes
Fatigue musculaire
Raideur musculaire
Douleur musculaire
Crampe musculaire
Myopathies
Âge
Variabilité des symptômes
Prévention
5
Prévention
Mode de vie sain
Exercice
Renforcement musculaire
Dépistage
Maladies héréditaires
Alimentation équilibrée
Nutriments
Repos
Récupération musculaire
Traitements
5
Physiothérapie
Traitement médicamenteux
Corticostéroïdes
Inflammation musculaire
Thérapie génique
Maladies musculaires héréditaires
Rééducation
Qualité de vie
Traitements expérimentaux
Thérapies ciblées
Complications
5
Complications
Perte de mobilité
Complications cardiaques
Myopathies
Infections
Faiblesse musculaire
Gestion des complications
Soins appropriés
Facteurs de risque
5
Facteurs de risque
Antécédents familiaux
Maladies auto-immunes
Myopathies
Mode de vie sédentaire
Facteurs de risque
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},
{
"@type": "Question",
"name": "Y a-t-il des risques de chutes ?",
"position": 23,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, la faiblesse musculaire augmente le risque de chutes et de blessures."
}
},
{
"@type": "Question",
"name": "Les infections sont-elles plus fréquentes ?",
"position": 24,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les patients peuvent être plus susceptibles aux infections en raison de la faiblesse."
}
},
{
"@type": "Question",
"name": "Les complications peuvent-elles être évitées ?",
"position": 25,
"acceptedAnswer": {
"@type": "Answer",
"text": "Certaines complications peuvent être évitées par une gestion proactive et des soins appropriés."
}
},
{
"@type": "Question",
"name": "Quels sont les facteurs de risque des maladies musculaires ?",
"position": 26,
"acceptedAnswer": {
"@type": "Answer",
"text": "Les facteurs incluent des antécédents familiaux, des infections et des traumatismes."
}
},
{
"@type": "Question",
"name": "L'âge est-il un facteur de risque ?",
"position": 27,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines maladies musculaires sont plus fréquentes avec l'âge."
}
},
{
"@type": "Question",
"name": "Le sexe influence-t-il le risque ?",
"position": 28,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, certaines maladies musculaires sont plus fréquentes chez les hommes que chez les femmes."
}
},
{
"@type": "Question",
"name": "Les maladies auto-immunes sont-elles un facteur ?",
"position": 29,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, les maladies auto-immunes peuvent augmenter le risque de myopathies."
}
},
{
"@type": "Question",
"name": "Le mode de vie influence-t-il le risque ?",
"position": 30,
"acceptedAnswer": {
"@type": "Answer",
"text": "Oui, un mode de vie sédentaire peut augmenter le risque de maladies musculaires."
}
}
]
}
]
}
Expert en Médecine, Optimisation des Parcours de Soins et Révision Médicale
Validation scientifique effectuée le 25/03/2026
Contenu vérifié selon les dernières recommandations médicales
5 publications dans cette catégorie
Publications dans "Maladies musculaires" :
3 publications dans cette catégorie
Affiliations :
From the Advanced Imaging Research Center (W.D.R., Y.A.B., I.A., E.O., B.M.), Department of Neurology (W.D.R., I.A., B.S.R., E.L.F.), Department of Biomedical Engineering (W.D.R.), Department of Behavioral Neuroscience (W.D.R., Y.A.B.), and Department of Pediatrics (B.S.R., E.L.F.), Oregon Health & Science University, Portland; Departments of Physical Therapy (W.T.T., S.C.F., R.J.W., H.A., C.S., D.J.L., K.V.), Statistics (S.C., M.J.D.), Physiology and Functional Genomics (A.B., G.A.W.), and Pharmacology & Therapeutics (H.L.S.), University of Florida, Gainesville; Department of Radiology (D.-J.W.) and Division of Neurology (G.T.), Children's Hospital of Philadelphia, PA; Department of Pediatrics (R.F.), Nemours Children's Hospital, Orlando, FL; and Shriners Hospital (B.S.R., E.L.F.), Portland, OR.
Publications dans "Maladies musculaires" :
3 publications dans cette catégorie
Affiliations :
Dubowitz Neuromuscular Centre, UCL Institute of Child Health & Great Ormond Street Hospital, London United Kingdom; NIHR Great Ormond Street Hospital Biomedical Research Centre, London, United Kingdom.
Publications dans "Maladies musculaires" :
3 publications dans cette catégorie
Affiliations :
College of Veterinary Medicine & Biomedical Sciences, Texas A&M University, College Station, Texas, USA.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
From the Advanced Imaging Research Center (W.D.R., Y.A.B., I.A., E.O., B.M.), Department of Neurology (W.D.R., I.A., B.S.R., E.L.F.), Department of Biomedical Engineering (W.D.R.), Department of Behavioral Neuroscience (W.D.R., Y.A.B.), and Department of Pediatrics (B.S.R., E.L.F.), Oregon Health & Science University, Portland; Departments of Physical Therapy (W.T.T., S.C.F., R.J.W., H.A., C.S., D.J.L., K.V.), Statistics (S.C., M.J.D.), Physiology and Functional Genomics (A.B., G.A.W.), and Pharmacology & Therapeutics (H.L.S.), University of Florida, Gainesville; Department of Radiology (D.-J.W.) and Division of Neurology (G.T.), Children's Hospital of Philadelphia, PA; Department of Pediatrics (R.F.), Nemours Children's Hospital, Orlando, FL; and Shriners Hospital (B.S.R., E.L.F.), Portland, OR.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
Krankenanstalt Rudolfstiftung Messerli Institute Vienna Austria.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
Pediatric Neurology, Università Cattolica del Sacro Cuore, Largo Gemelli 8, 00168 Rome, Italy; Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy. Electronic address: eugeniomaria.mercuri@unicatt.it.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
Department of Neurology, University of Rochester, Rochester, New York.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
Department of Neurology, University of Rochester Medical Center, Rochester, New York, USA.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
Center for Genetic Medicine Research, Children's National Medical Center, Washington, DC, USA.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
John Walton Muscular Dystrophy Research Centre, Newcastle University, Newcastle upon Tyne, UK.
Division of Neurology, Department of Medicine, The Ottawa Hospital, Ottawa, Canada.
Brain and Mind Research Institute, University of Ottawa, Ottawa, Canada.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
From the Department of Neurology (R.J.M.G., K.M., C.R.v.K., T.H.A.S., C.E.E., G.W.P., N.C.V., B.G.M.v.E.), Donders Center for Neuroscience, Radboud University Medical Center, Nijmegen; Department of Human Genetics (R.J.L.F.L., S.M.v.d.M.), Leiden University Medical Center, the Netherlands; and Department of Neurology (J.M.S.), Kansas University Medical Center, Kansas City.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
From the Department of Neurology (R.J.M.G., K.M., C.R.v.K., T.H.A.S., C.E.E., G.W.P., N.C.V., B.G.M.v.E.), Donders Center for Neuroscience, Radboud University Medical Center, Nijmegen; Department of Human Genetics (R.J.L.F.L., S.M.v.d.M.), Leiden University Medical Center, the Netherlands; and Department of Neurology (J.M.S.), Kansas University Medical Center, Kansas City.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
From the Department of Neurology (R.J.M.G., K.M., C.R.v.K., T.H.A.S., C.E.E., G.W.P., N.C.V., B.G.M.v.E.), Donders Center for Neuroscience, Radboud University Medical Center, Nijmegen; Department of Human Genetics (R.J.L.F.L., S.M.v.d.M.), Leiden University Medical Center, the Netherlands; and Department of Neurology (J.M.S.), Kansas University Medical Center, Kansas City.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
From the Department of Neurology (R.J.M.G., K.M., C.R.v.K., T.H.A.S., C.E.E., G.W.P., N.C.V., B.G.M.v.E.), Donders Center for Neuroscience, Radboud University Medical Center, Nijmegen; Department of Human Genetics (R.J.L.F.L., S.M.v.d.M.), Leiden University Medical Center, the Netherlands; and Department of Neurology (J.M.S.), Kansas University Medical Center, Kansas City.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
Department of Electrical and Computer Engineering, Texas A&M University, College Station, Texas, USA.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
Department of Electrical and Computer Engineering, Texas A&M University at Qatar, Doha, Qatar.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
College of Veterinary Medicine & Biomedical Sciences, Texas A&M University, College Station, Texas, USA.
Publications dans "Maladies musculaires" :
2 publications dans cette catégorie
Affiliations :
College of Veterinary Medicine & Biomedical Sciences, Texas A&M University, College Station, Texas, USA.
Publications dans "Maladies musculaires" :
Pathophysiological analysis and drug discovery targeting human diseases require disease models that suitably recapitulate patient pathology. Disease-specific human induced pluripotent stem cells (hiPS...
Oculopharyngodistal myopathy (OPDM) is an autosomal dominant myopathy clinically characterized by distal muscle weakness. Even though the identification of four causative genes, LRP12, GIPC1, NOTCH2NL...
Axial muscle CT and/or T1-weighted MRI data from 54 genetically confirmed patients with OPDM (OPDM_LRP12; n = 43, OPDM_GIPC1; n = 6, OPDM_NOTCH2NLC; n = 5) and 57 with OPMD were evaluated. We scored t...
All OPDM subtypes showed a similar pattern of distribution in the affected muscles; soleus and medial gastrocnemius involved in the early stage, followed by tibialis anterior and extensor digitorum lo...
We identified a diagnostic muscle involvement pattern in OPDM reflecting its natural history. The results of this study will help in the appropriate intervention based on the diagnosis of OPDM, includ...
A 62-year-old man presented with a 5-year history of progressive myasthenia, myalgia, and skin changes. Upon laboratory testing, elevated serum creatine kinase and lactate dehydrogenase, as well as mo...
Statins are a mainstay intervention for cardiovascular disease prevention, yet their use can cause rare severe myopathy. HMG-CoA reductase, an essential enzyme in the mevalonate pathway, is the target...
Mitogen-activated protein kinase 8-interacting protein 3 gene (MAPK8IP3) encodes the c-Jun-amino-terminal kinase-interacting protein 3 (JIP3) and is involved in retrograde axonal transport. Heterozygo...
Limb-girdle muscular dystrophy R8 (LGMD R8) is a rare autosomal recessive muscle disease caused by TRIM32 gene biallelic defects. The genotype-phenotype correlation of this disease has been reported p...
We performed whole-genome sequencing (WGS) and Sanger sequencing on the proband. Meanwhile, the function of mutant TRIM32 protein was analyzed by bioinformatics and experimental analysis. In addition,...
The two patients displayed typical symptoms of LGMD R8, which worsened during pregnancy. Genetic analysis by whole-genome sequencing (WGS) and Sanger sequencing showed that the patients were compound ...
This research extended the spectrum of TRIM32 mutations and firstly provided useful data on the genotype-phenotype correlation, which is valuable for the accurate diagnosis and genetic counseling of L...
Alcohol-related myopathy is one of the earliest alcohol-associated pathological tissue changes that is progressively exacerbated by cumulative long-term alcohol misuse. Acute and chronic alcohol use l...
This review focuses on peer-reviewed manuscripts published between January 2012 and November 2022 using the search terms "alcohol" or "ethanol" and "skeletal muscle" in MEDLINE, PubMed, and Web of Sci...
Eligible manuscripts included full-length research papers that discussed acute and chronic effects of alcohol on skeletal muscle mass and function in both clinical and preclinical studies. The review ...
Both acute and chronic alcohol use decrease protein synthesis and increase protein degradation. Alcohol also impairs mitochondrial function and extracellular matrix remodeling. However, there is a gap...
Cylindrical spirals (CSs) are ultrastructurally distinct, intracytoplasmic inclusions characterized by concentrically wrapped lamellae, which are rarely found in skeletal muscle biopsies on electron m...
Mutations in the gene encoding valosin-containing protein (VCP) are related to myriad medical conditions, including familial amyotrophic lateral sclerosis, inclusion body myopathy, and frontotemporal ...
We report a 53-year-old PD patient with VCP mutation who later developed motor complications, thus receiving subthalamic nucleus deep brain stimulation (DBS) at the age of 56 years. However, myopathy ...
With the phenotype variability of VCP, DBS should be carefully evaluated, considering the possible unfavorable long-term outcomes due to other symptoms of this mutation....
Neutral lipid-storage disease with myopathy (NLSDM) is an autosomal recessive neuromuscular disorder caused by mutations in PNPLA2, and the average age at onset is 30 years. To date, only eight patien...