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2,126 Possible Causes for Muscular Atrophy, Possibly Scoliosis

Did you mean: Muscular Atrophy, Possibly, Scoliosis

  • Syringomyelia

    It results in neurological deficits that generally consist of segmental muscular weakness and atrophy accompanied by a dissociated sensory loss (loss of pain and temperature[] Risks of surgery are substantial, with possible neurologic progression.[] Syringomyelia is marked clinically by pain and PARESTHESIA, muscular atrophy of the hands, and analgesia with thermoanesthesia of the hands and arms, but with the tactile[]

  • 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[] What's New in the Management of Neuromuscular Scoliosis. J Pediatr Orthop. 2016 Sep. 36 (6):627-33. [Medline].[] muscular dystrophy Spinal muscular atrophy (SMA) Myotonia congenita Myotonic dystrophy Charcot Marie Tooth disease (hereditary sensory motor neuropathy) At the Pediatric[]

  • Scoliosis

    […] dystrophy and spinal muscular atrophy).[] We hypothesized that augmented sensory feedback and strength exercises could be an important stage in a rehabilitation program aimed at hindering, or possibly reversing, scoliosis[] Epidural pneumorrhachis is a possible complication of scoliosis surgery with pedicle screw fixation, which can result in the intraoperative loss of neuromonitoring signals[]

  • Friedreich Ataxia

    atrophy, Dr.[] Orthopedic problems such as foot deformities and scoliosis can be treated with braces or surgery.[] atrophy and related syndromes G12.0 Infantile spinal muscular atrophy, type I [Werdnig-Hoffman] G12.1 Other inherited spinal muscular atrophy G12.2 Motor neuron disease Reimbursement[]

  • Spinal Muscular Atrophy Type 3

    Spinal muscular atrophies (SMAs) are neurodegenerative disorders caused by mutations in the survival motor neuron 1 (SMN1) gene.[] Carmell mom to Kara, idiopathic scoliosis, Blake 19, GERD and Braydon 14, VACTERL, GERD, DGE, VEPTR #137, thoracic insufficiency, rib anomalies, congenital scoliosis, missing[] Best practice guidelines for molecular analysis in spinal muscular atrophy. Eur J Hum Genet. 2001;9(7):484-91. D'Amico A, et al. Spinal muscular atrophy.[]

  • Congenital Muscular Dystrophy

    The objectives of this study were to determine the effects that routine daily home air-stacking maneuvers have on pulmonary function in patients with spinal muscular atrophy[] Some patients with mild FCMD can sit at the age of puberty, but progression to scoliosis is possible.[] atrophy, forms of Ehlers-Danlos syndrome, and Marfan syndrome (see these terms).[]

  • Hereditary Motor and Sensory Neuropathy

    Charcot-Marie-Tooth disease Déjérine-Sottas disease Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal[] There can be high arched feet, hammer toes, foot drop, and foot deformities, and possibly scoliosis. Who gets Hereditary Motor Sensory Neuropathy?[] It may be possible to palpate enlarged and excessively firm nerves.[]

  • Adult Spinal Muscular Atrophy

    […] spinal muscular atrophy and juvenile asymmetric segmental spinal muscular atrophy.[] The aims of an exercise programme are to:- Maintain safe ambulation for as long as possible.[] Spinal muscular atrophies of childhood Spinal muscular atrophy Spinal muscular atrophy Spinal muscular atrophy Spinal muscular atrophy Spinal muscular atrophy Spinal muscular[]

  • 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[] This case series highlights important surgical strategies that can be utilized to treat scoliosis in patients with SMA.[] Twenty-five patients had scoliosis and eight of these patients received surgical treatment for scoliosis with improvement in clinical outcomes.[]

  • Becker Muscular Dystrophy

    BACKGROUND/PURPOSE: The purpose of this study was to explore the prevalence, nature and scope of pain in adolescents with spinal muscular atrophy and Duchenne and Becker muscular[] Electrocardiogram (ECG) and echocardiogram - these may be difficult to interpret due to scoliosis.[] muscular atrophy (SMA).[]

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