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462 Possible Causes for Muscular Atrophy, Unable to Stand

  • Muscular Dystrophy

    Distal muscular dystrophies are a group of inherited primary muscle disorders showing progressive weakness and atrophy preferentially in the hands, forearm, lower legs, or[ncbi.nlm.nih.gov] […] or stand without help.[healthline.com] muscular dystrophy Spinal muscular atrophy (SMA) Myotonia congenita Myotonic dystrophy Charcot Marie Tooth disease (hereditary sensory motor neuropathy) At the Pediatric[ynhh.org]

  • Guillain-Barré Syndrome

    RESULTS: All six patients had different degrees of muscular atrophy at nadir and in two, respiratory muscles were involved.[ncbi.nlm.nih.gov] Patients may be unable to stand or walk despite reasonable strength, especially when ophthalmoparesis or impaired proprioception is present.[emedicine.medscape.com] The peroneal muscular atrophy syndrome 8. The ataxic neuropathies 9. Sensory neuropathies 10. Neuropathies in metabolic and degenerative disorders 11.[scinapse.io]

  • Spinal Muscular Atrophy

    […] muscle atrophy survival motor neuron spinal muscular atrophy spinal muscular atrophies of childhood Spinal muscular atrophy Statements spinal-muscular-atrophy-pro Identifiers[wikidata.org] Children can sit without support but are unable to stand or walk unaided. Children also may have respiratory difficulties.[ninds.nih.gov] They are able to sit without support but are unable to stand or walk unaided, and some may lose the ability to stay seated independently over time without treatment.[ninds.nih.gov]

  • Limb-Girdle Muscular Dystrophy

    They are usually unable to stand without using their own body to steady themselves and, as such, present with Gower’s sign (where patients use their own hands to push off[lecturio.com] atrophy.[ncbi.nlm.nih.gov] […] by Duchenne.1,2 Other descriptions followed: familial atrophy of the pelvic girdle muscles (Leyden in 1876), scapulohumeral muscular atrophy (Erb in 1884), and myopathy with[dash.harvard.edu]

  • Polymyositis

    Kennedy disease or X-linked spinobulbar muscular atrophy is a rare X-linked recessive disorder with clinical features of slowly progressive atrophy and weakness of limb and[ncbi.nlm.nih.gov] atrophy).[ncbi.nlm.nih.gov] MDA addresses the muscular dystrophies, spinal muscular atrophy, ALS, Charcot-Marie-Tooth disease, myasthenia gravis, Friedreich's ataxia, metabolic diseases of muscle, and[brainfacts.org]

  • Dermatomyositis

    atrophy).[ncbi.nlm.nih.gov] MDA addresses the muscular dystrophies, spinal muscular atrophy, ALS, Charcot-Marie-Tooth disease, myasthenia gravis, Friedreich's ataxia, metabolic diseases of muscle, and[brainfacts.org] Of them, 81.4% (105/129) showed a visible inflammatory muscular edema on their WBMRI; 29.5% (38/129) had varying degrees of fatty infiltration (9 cases with clear muscular[ncbi.nlm.nih.gov]

  • Motor Neuron Disease

    Some MNDs, such as ALS and some forms of spinal muscular atrophy, are fatal.[ninds.nih.gov] The ALS features of the disorder eventually render patients unable to stand, walk, get in or out of bed on their own, or use their hands and arms.[theaftd.org] Unable to stand 2 years SMA 3 Kugelberg-Welander disease 18 months-3 years Able to stand and walk Adult SMA 4 Adult Able to stand and walk Adult SMA muscle SMA.[neuropathology-web.org]

  • Poliomyelitis

    We report the case of PPS in a patient, 40 years, that thirty-five years after had had paralytic poliomyelitis, developed new symptoms of fatigue, muscular atrophy, dyspnea[ncbi.nlm.nih.gov] Some of these patients develop post-poliomyelitis muscular atrophy (PPMA) which is characterized by a slowly progressive muscle weakness.[ncbi.nlm.nih.gov] Some of these patients develop slowly progressive muscle weakness known as post-poliomyelitis muscular atrophy (PPMA).[ncbi.nlm.nih.gov]

  • 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] Unable to stand 2 years SMA 3 Kugelberg-Welander disease 18 months-3 years Able to stand and walk Adult SMA 4 Adult Able to stand and walk Adult SMA muscle SMA.[neuropathology-web.org] Children may be able to sit but are unable to stand or walk unaided, and may have respiratory difficulties. The progression of disease is variable.[web.archive.org]

  • Primary Lateral Sclerosis

    This locus had not been implicated in ALS or in hereditary spastic parapareses, spinal muscular atrophy, or spinal and bulbar muscular atrophy. [7] A genetically mediated[emedicine.com] The patient may be unable to stand up from a chair without help.[the-medical-dictionary.com] Continued Spinal Muscular Atrophy This is an inherited condition that affects lower motor neurons. A defect in a gene called SMN1 causes spinal muscular atrophy.[webmd.com]

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