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75 Possible Causes for Facial Muscle Weakness and Progressive Atrophy, Muscle Spasticity, Muscular Atrophy

  • Amyotrophic Lateral Sclerosis

    The patients were a 54-year-old man with progressive muscular atrophy who underwent removal of internal fixators in the arm and leg, and a 66-year-old woman with amyotrophic[ncbi.nlm.nih.gov] This is a progressive and fatal disease, with initial complaints about muscle spasticity followed by progressively worsening muscle weakness.[fusfoundation.org] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org]

  • Upper Motor Neuron Disease

    atrophy(PMA), Progressive bulbar palsy(PBP), MEPs were recorded from abductor pollicis brevis and abductor hallucis.[e-acn.org] , in particular the limbs, where movement becomes more and more difficult The limb muscles begin to shrink and some develop spasticity, where they become stiff Pain in the[newhealthadvisor.com] Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy.[advancedpsy.com]

  • Myotonic Dystrophy

    Neuromuscular disorders like myotonic dystrophy (dystrophia myotonica or Steinert's disease) and spinal muscular atrophy are associated with perioperative complications related[ncbi.nlm.nih.gov] Clinical Presentation: Variable, progressive disability; facial and distal limb muscle weakness with myotonia; cataracts; cardiac conduction defects; diabetes mellitus; and[ajnr.org] New contributions to the theory of muscular atrophy in supranuclear paralysis especially in cerebral hemiplegia (Habilitationsschrift).[doi.org]

  • Motor Neuron Disease

    Some MNDs, such as ALS and some forms of spinal muscular atrophy, are fatal.[ninds.nih.gov] Involvement of UMN results in stiffness of muscles (spasticity) and slowed movements.[mndnsw.asn.au] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org]

  • Progressive Bulbar Palsy

    […] term(s): Adult form spinal muscular atrophy Childhood form, type II spinal muscular atrophy Distal spinal muscular atrophy Juvenile form, type III spinal muscular atrophy[icd10coded.com] Patients who also have ALS experience a gradual onset of its symptoms, which include clumsiness, fatigue, loss of muscle control and spasticity, as the ALS Association describes[reference.com] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[secure.ssa.gov]

  • Lower Motor Neuron Syndrome with Late-Adult Onset

    muscular atrophy, but have different genetic causes.[togetherinsma.com] Doctors can prescribe medications for reducing fatigue, muscle cramps, muscle spasticity, and excessive saliva or phlegm, as well as pain, depression, sleeping problems or[livescience.com] Symptoms include pharyngeal muscle weakness (muscles that are involved in swallowing), weak facial muscles, progressive loss of speech, and tongue muscle atrophy.[advancedpsy.com]

  • Progressive Muscular Atrophy

    The name "spinal muscular atrophy" is ambiguous as it refers to any of various spinal muscular atrophies, including the autosomal recessive spinal muscular atrophy caused[en.wikipedia.org] Symptoms are similar to the common form of ALS, though spasticity is absent and muscle weakness is less… Read More[britannica.com] Symptoms include pharyngeal muscle weakness (involved with swallowing), weak jaw and facial muscles, progressive loss of speech, and tongue muscle atrophy.[web.archive.org]

  • Autosomal Recessive Lower Motor Neuron Disease with Childhood Onset

    […] are not associated with a defect in the SMN1 gene on chromosome 5q X-linked spinal muscular atrophy X-linked spinal muscular atrophy is seen only among males![amboss.com] Constipation Occured due to pelvic muscle weakness, improper diet, spasticity, as well as drugs such as anticholinergics and opioids.[5].[explainmedicine.com] Spinal muscular atrophy is characterised by slowly progressive muscle weakness and atrophy of the limb muscles associated with motor neurone loss in the spinal cord.[patient.info]

  • Multifocal Motor Neuropathy

    Abstract Multifocal motor neuropathy (MMN) and progressive muscular atrophy (PMA) are associated with IgM monoclonal gammopathy or the presence IgM anti-GM1-antibodies.[ncbi.nlm.nih.gov] Patients with motor neuropathies may have preserved reflexes in weak muscles, but overt spasticity and bulbar features are conspicuously lacking.[neuromuscular.wustl.edu] In the first patient the symptoms were slowly progressive with bulbar muscle impairment, generalized weakness, muscular atrophy with cramps and fasciculations.[moh-it.pure.elsevier.com]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    Treatment for spinal muscular atrophy Unfortunately, there is currently no specific treatment for SMA.[betterhealth.vic.gov.au] The small muscles of the hands and feet are usually first affected, but muscle spasticity is absent. Primary lateral sclerosis - this is another rare type of MND.[patient.info] weakness DHMN8 600175 TRPV4 12q24.11 Autosomal dominant Congenital distal spinal muscular atrophy Affects primarily distal muscles of lower limbs, non-progressive, rare DHMNJ[en.wikipedia.org]

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