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237 Possible Causes for Mild Facial Muscle Weakness, Myopathy

  • Muscular Dystrophy

    Mild involvement of the facial musculature (particularly of the orbicularis oculi and oris muscles) is often present.[orpha.net] Nemaline myopathy Nemaline myopathy. Clusters of rod bodies. Gomori trichrome. Nemaline myopathy Nemaline myopathy. EM.[neuropathology-web.org] Muscle weakness of the face is common, and may include: Eyelid drooping Inability to whistle Decreased facial expression Depressed or angry facial expression Difficulty pronouncing[web.archive.org]

  • Inclusion Body Myositis

    Facial muscles are unaffected in PM and DM, but mild facial muscle weakness is common in patients with IBM.[accessmedicine.mhmedical.com] The comorbidity of inclusion body myositis and sarcoid myopathy is rare.[ncbi.nlm.nih.gov] There is early weakness and atrophy of forearms and quadriceps and a third of patients also have mild facial weakness.[ncbi.nlm.nih.gov]

  • Facioscapulohumeral Muscular Dystrophy

    […] and mild lower facial weakness.[ncbi.nlm.nih.gov] OBJECTIVES: To report cases of chronic autoimmune necrotizing myopathy with anti-signal recognition particle antibodies (anti-SRP myopathy) initially misdiagnosed as muscular[ncbi.nlm.nih.gov] The 53-year-old mother of the proband had limb-girdle (L-G) type muscular weakness with very mild facial involvement.[ncbi.nlm.nih.gov]

  • Polymyositis

    Facial muscles are unaffected in PM and DM, but mild facial muscle weakness is common in patients with IBM.[accessmedicine.mhmedical.com] Furthermore, glucocorticosteroid (GC) toxicity leads to a significant disability known as steroid myopathy, particularly in elderly patients.[ncbi.nlm.nih.gov] myopathies.[ncbi.nlm.nih.gov]

  • Oculopharyngeal Muscular Dystrophy

    Ptosis and mild facial and proximal muscle weakness were present by 9 years of age.[ncbi.nlm.nih.gov] […] some ultrastructural characteristics with distal myopathy with rimmed vacuoles and hereditary inclusion body myopathy.[ncbi.nlm.nih.gov] The question whether oculopharyngodistal myopathy (MIM 164310) is a distinct disease entity or a variant of oculopharyngeal muscular dystrophy (MIM 164300) persists.[ncbi.nlm.nih.gov]

  • Central Core Disease

    The symptoms of CCD are variable, but usually involve hypotonia (decreased muscle tone) at birth, mild delay in child development (highly variable between cases), weakness[en.wikipedia.org] This review will focus on myotubular myopathy, centronuclear myopathy, central core disease, and congenital neuromuscular disease with uniform Type 1 fiber, myopathies that[ncbi.nlm.nih.gov] Nemaline myopathy: moderate weakness of voluntary muscles in the arms, legs, and trunk; mild weakness of facial muscles; delays in reaching developmental motor milestones[medical-dictionary.thefreedictionary.com]

  • Secondary Myopathy

    Mild facial weakness may be seen even when limb weakness is relatively mild (rare in DM and PM), and dysphagia can be an early or late feature.[jnnp.bmj.com] We present a family with a distal myopathy secondary to a mutation in myotilin.[eprints.soton.ac.uk] Mild facial weakness, neck weakness usually occurs.[sites.google.com]

  • Bacterial Myositis

    Facial muscles are unaffected in PM and DM, but mild facial muscle weakness is common in patients with IBM.[accessmedicine.mhmedical.com] Acquired myopathies can be subclassified as inflammatory myopathies, toxic myopathies, and myopathies associated with systemic conditions.[clevelandclinicmeded.com] Proximal myopathy gradually improved on HAART.[adc.bmj.com]

  • Nemaline Myopathy

    muscle weakness have been observed 8 as seen in our patient, 18 months after symptom onset.[jamanetwork.com] Nemaline myopathy is divided into six types.[ghr.nlm.nih.gov] Clinical examination on presentation at the age of 40 revealed a facial weakness, atrophy and weakness of the arm muscles and distal leg muscles with mild contractures of[ncbi.nlm.nih.gov]

  • Erb Muscular Dystrophy

    Affected individuals develop weakness of the lower limbs that may be mild or severe. Weakness of facial muscles may also occur.[rarediseases.org] 4, 5 Tropomyosin Hypertrophic cardiomyopathy 3 Nemaline myopathy 1 Titin Hypertrophic cardiomyopathy 9 Other Fibrillin Marfan syndrome Weill–Marchesani syndrome Filamin FG[en.wikipedia.org] , ocular Mitochondrial ocular myopathy Muscular dystrophy Muscular dystrophy, distal Muscular dystrophy, Duchenne Muscular dystrophy, Emery Dreifuss Muscular dystrophy, Erbs[icd9data.com]

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