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110 Possible Causes for Facial Muscle Weakness and Progressive Atrophy, Muscular Atrophy, Scoliosis

  • 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] What's New in the Management of Neuromuscular Scoliosis. J Pediatr Orthop. 2016 Sep. 36 (6):627-33. [Medline].[emedicine.medscape.com] Abstract Facioscapulohumeral muscular dystrophy is an autosomal-dominant, slowly progressive myopathy that involves facial, shoulder, and upper arm muscles.[ncbi.nlm.nih.gov]

  • 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] This case series highlights important surgical strategies that can be utilized to treat scoliosis in patients with SMA.[ncbi.nlm.nih.gov] 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]

  • Spinal Muscular Atrophy Type 1

    atrophy type 1 with paradoxical breathing were placed on high-span PIP PEEP when sleeping from the point of diagnosis of spinal muscular atrophy.[ncbi.nlm.nih.gov] Scoliosis occurs as a child with type 2 grows and gets bigger. There is no specific life span.[stopsma.org] We present a baby with spinal muscular atrophy type 1, an inherited disorder causing progressive weakness, leading to complete paralysis of respiratory, facial and limb muscles[ncbi.nlm.nih.gov]

  • Spinal Muscular Atrophy Type 3

    Spinal muscular atrophies (SMAs) are neurodegenerative disorders caused by mutations in the survival motor neuron 1 (SMN1) gene.[symptoma.com] Carmell mom to Kara, idiopathic scoliosis, Blake 19, GERD and Braydon 14, VACTERL, GERD, DGE, VEPTR #137, thoracic insufficiency, rib anomalies, congenital scoliosis, missing[scoliosis.org] 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]

  • Scapuloperoneal Spinal Muscular Atrophy

    We previously described a large New England kindred exhibiting an autosomal dominant neurogenic SP syndrome (scapuloperoneal spinal muscular atrophy, SPSMA).[ncbi.nlm.nih.gov] Additional features, such as vocal cord paralysis, scoliosis and/or arthrogryposis, are likely to occur.[ncbi.nlm.nih.gov] Scapuloperoneal spinal muscular atrophy: Type 1 (AD form) appears at age 14-26, with weakness, distal leg atrophy, and absent tendon reflexes and sparing of intrinsic foot[emedicine.medscape.com]

  • Adult Spinal Muscular Atrophy

    […] spinal muscular atrophy and juvenile asymmetric segmental spinal muscular atrophy.[symptoma.com] Corrective straps stretch feet, knees & hips and reduce asymmetry and tilting of the pelvis which can lead to scoliosis.[daneverard.co.uk] 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]

  • Muscular Atrophy

    - muscle Amyotrophia edit English muscular atrophy human disease Amyotrophia NOS Amyotrophia NOS (disorder) Muscle atrophy (disorder) Muscle wasting Muscular atrophy Wasting[wikidata.org] […] variable clinical phenotype that comprises arthrogryposis, spontaneously resolving respiratory insufficiency at birth, muscular atrophy predominantly of the distal lower limbs, scoliosis[ncbi.nlm.nih.gov] 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]

  • Distal Spinal Muscular Atrophy Type 3

    Homepage Rare diseases Search Search for a rare disease X-linked distal spinal muscular atrophy type 3 Disease definition X-linked distal spinal muscular atrophy type 3 is[orpha.net] Oftentimes scoliosis is present in patients with Type 3 or Type 4 SMA.[sinicropispine.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]

  • Spinal Muscular Atrophy with Respiratory Distress Type 1

    Homepage Rare diseases Search Search for a rare disease Spinal muscular atrophy with respiratory distress type 1 Disease definition Spinal muscular atrophy with respiratory[orpha.net] 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] Hardart MK, Truog RD (2003) Spinal muscular atrophy-type I.[doi.org]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    Homepage Rare diseases Search Search for a rare disease X-linked distal spinal muscular atrophy type 3 Disease definition X-linked distal spinal muscular atrophy type 3 is[orpha.net] Orthopedic • Considerations: • Scoliosis • SMA2 SMA3 SMA1 • Early onset: 4-9 y • Bracing may slow progression, but wont stop it • Bracing may decrease tidal breathing if not[slideshare.net] 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]

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