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8 Possible Causes for Scoliosis (Onset around Puberty)

Did you mean: Scoliosis (Onset around Puberty

  • Congenital Myopathy with Excess of Thin Filaments

    […] de Winter, J. M., Buck, D., Hidalgo, C., Jasper, J. R., Malik, F. I., Clarke, N. F., ... Granzier, H. (2013). Troponin activator augments muscle force in nemaline myopathy patients with nebulin mutations. Journal of Medical Genetics, 50 (6), 383-392. de Winter, J.M. ; Buck, D. ; Hidalgo, C. ; Jasper, J.R. ; Malik, F.I. ; Clarke, N.F. ;[…][research.vu.nl]

  • Ataxia

    His initial reports noted that the age of onset was around puberty and ataxia, dysarthria, sensory loss, muscle weakness, scoliosis, foot deformity, and cardiac symptoms were[jmg.bmj.com]

  • Degenerative Disorder

    His initial reports noted that the age of onset was around puberty and ataxia, dysarthria, sensory loss, muscle weakness, scoliosis, foot deformity, and cardiac symptoms were[doi.org]

  • Generalized Myotonia of Thomsen

    Disease onset is usually around puberty, but it may vary from infancy to adulthood. There is no cure for FA so far.[ataxia-study-group.net] […] dysarthria (slurred speech), spasticity, deep sensory loss, muscular weakness primarily affecting the lower limbs, visual and auditory loss, and skeletal deformities (e.g. scoliosis[ataxia-study-group.net]

  • Friedreich Ataxia

    Disease onset is usually around puberty, but it may vary from infancy to adulthood. There is no cure for FA so far.[ataxia-study-group.net] His initial reports noted that the age of onset was around puberty and ataxia, dysarthria, sensory loss, muscle weakness, scoliosis, foot deformity, and cardiac symptoms were[doi.org] […] dysarthria (slurred speech), spasticity, deep sensory loss, muscular weakness primarily affecting the lower limbs, visual and auditory loss, and skeletal deformities (e.g. scoliosis[ataxia-study-group.net]

  • Nemaline Myopathy Type 2

    (Photo : You Tracker) A structural illustration shows the protein leiomodin 2 (magenta ribbons) and two actin subunits Rice Univeristy and Baylor College researchers have unlocked the first structural map of a protein (leiomodin 2) in order to treat a neuromuscular disease. This study could improve and help to[…][sciencetimes.com]

  • Spondyloepimetaphyseal Dysplasia Type Pakistani

    The condition typically manifests around puberty with a short neck, scoliosis or thoracic kyphosis, lumbar hyperlordosis, and early-onset progressive osteoarthritis of the[orpha.net]

  • Spondyloepiphyseal Dysplasia Type Byers

    The condition typically manifests around puberty with a short neck, scoliosis or thoracic kyphosis, lumbar hyperlordosis, and early-onset progressive osteoarthritis of the[orpha.net]

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