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153 Possible Causes for Electromyogram Abnormal, No Muscle Weakness, Scoliosis

  • Muscular Dystrophy

    What's New in the Management of Neuromuscular Scoliosis. J Pediatr Orthop. 2016 Sep. 36 (6):627-33. [Medline].[] It causes progressive weakness in muscles of the face, arms, legs, and around the shoulders and chest.[] From Wikidata Jump to navigation Jump to search myopathy characterized by progressive skeletal muscle weakness degeneration edit English muscular dystrophy myopathy characterized[]

  • Duchenne Muscular Dystrophy

    Muscle weakness Other names Myasthenia Specialty Neurology Muscle weakness is a lack of muscle strength.[] One of them showed severe scoliosis. After hospitalization chest CT scan revealed extensive pulmonary bilateral segmental atelectasis.[] Ages at loss of ambulation or scoliosis diagnosis did not differ statistically among treatment groups.[]

  • Spinal Muscular Atrophy Type 1

    Scoliosis occurs as a child with type 2 grows and gets bigger. There is no specific life span.[] An EMG can detect abnormal electrical muscle activity due to diseases and neuromuscular conditions.[] AIM: This study described end-of-life care for children affected by spinal muscular atrophy type 1 (SMA1), which is characterised by progressive muscle weakness and develops[]

  • Muscular Atrophy

    […] variable clinical phenotype that comprises arthrogryposis, spontaneously resolving respiratory insufficiency at birth, muscular atrophy predominantly of the distal lower limbs, scoliosis[] An EMG can detect abnormal electrical muscle activity due to diseases and neuromuscular conditions.[] Limb girdle weakness, twitching, lack of reflexes, and weakness of tongue, face, and neck muscles are seen.[]

  • Spinal Muscular Atrophy Type 3

    EMOTAS study aim to understand if NMJ abnormalities could have an impact on motor performance and fatigue in SMA type 3 ambulatory patients by electromyogram and to improve[] Swallowing muscle weakness : Infants with swallowing or sucking weakness can be fed with a gastrostomy tube.[] Carmell mom to Kara, idiopathic scoliosis, Blake 19, GERD and Braydon 14, VACTERL, GERD, DGE, VEPTR #137, thoracic insufficiency, rib anomalies, congenital scoliosis, missing[]

  • Becker Muscular Dystrophy

    Progressive scoliosis and contracture formation may require surgical intervention.[] […] changes in the structure of the muscle cells Tests that stain the muscle sample can be used to visualize any muscle proteins present Electromyogram (EMG): Another diagnostic[] Later symptoms Muscle weakness: Affects the proximal muscles of the limbs mainly.[]

  • Limb-Girdle Muscular Dystrophy

    Scoliosis - occurs mainly after wheelchair dependence. Careful attention to seating is important.[] However, most patients in the current family showed distal as well as proximal limb weakness rather than weakness of toe and finger flexor muscles that were typical features[] Other services, such as orthopedic surgery (for scoliosis or contractures) or cardiology (for abnormal heart rhythms or impaired cardiac function), are available as needed[]

  • Progressive Muscular Atrophy

    Scoliosis and other spinal deformities are often diagnosed in people who show CMT at an early age and some people experience hip and knee dislocations while some are born[] She developed muscle weakness of the distal part of the left lower extremity at age 42, followed by muscle weakness and atrophy of the right lower extremity and upper extremities[] Kids with SMA can develop scoliosis (a curved spine) if the back muscles are weak.[]

  • Myopathy

    The proband showed foot drop, scoliosis, and winged scapula, while his mother only showed mild foot drop and winged scapula.[] Electroencephalographic abnormalities have been noted in several patients with the early-onset form of the disease before clinically apparent seizure activity begins.[] Muscle weakness regressed and dysphagia disappeared with treatment.[]

  • Facioscapulohumeral Muscular Dystrophy

    BACKGROUND: Although muscle weakness is a hallmark of facioscapulohumeral muscular dystrophy (FSHD), the molecular mechanisms that lead to weakness in FSHD remain largely[] Wheelchair-dependent patients with (kypho-)scoliosis showed the most restricted lung function.[] Preoperative examination showed hyperlordosis of 116 with scoliosis of 44 . Posterior correction and bone graft fusion was performed.[]

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