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136 Possible Causes for Congenital Non-Progressive Myopathy

  • Chudley-Rozdilsky Syndrome

    The only two patients ever described suffered from a congenital non-progressive myopathy of type multiminicore myopathy, severe mental retardation, short stature and facial[] Congenital nonprogressive myopathy with Moebius and Robin sequences - See Carey-Fineman-Ziter syndrome Congenital non-progressive peripheral neuropathy with arthrogryposis[] The affected siblings were children of a consanguineous couple and suffered from a congenital, non-progressive myopathy associated with generalized weakness that has been[]

  • Central Core Disease

    Register A NEW CONGENITAL NON-PROGRESSIVE MYOPATHY - 24 Hours access EUR 36.00 GBP 28.00 USD 45.00 Rental This article is also available for rental through DeepDyve.[]

  • Congenital Fiber-Type Disproportion Myopathy

    Congenital myopathy with type 1 fiber predominance (CMT1P) is also a distinct entity of congenital myopathy characterized by non-progressive childhood neuromuscular disorders[] ; the disease course is variable but most are non-progressive and some patients will have normal life expectancies.[] Congenital myopathy with fiber type disproportion (CFTD) is an established disorder of congenital myopathy.[]

  • Multicore Myopathy with External Ophthalmoplegia

    non-progressive myopathy, associated with scoliosis.[] A NEW CONGENITAL NON-PROGRESSIVE MYOPATHY Denborough, M. A.; Dennett, X; Anderson, R. M. (1973). "Central-core disease and malignant hyperpyrexia".[] ., Multicore myopathy, microcephaly aganglionosis, and short stature (1994) J Child Neurol, 9, pp. 275-277. , Abstractpt_BR dc.description.referenceKumano, K., Congenital[]

  • Arthrogryposis due to Muscular Dystrophy

    Magee : A new congenital non-progressive myopathy. Brain 79, 610 (1956). Google Scholar — W. K. Engel , J. E. Somers , and T. Wanko : Nemaline myopathy.[] .: Congenital muscular dystrophy. A case report with autopsy findings. Neurology (Minneap.) 13, 526 (1963). Google Scholar Shy , G. M., and K. R.[] A new congenital myopathy. Brain 86, 793 (1963). Google Scholar Spiro, A. J., G. M. Shy , and N. K. Gonatas : Myotubular myopathy. Arch. Neurol. (Chic.) 14, 1 (1966).[]

  • Familial Recurrent Peripheral Facial Palsy

    congenital disorder of glycosylation with intellectual disability as a major feature Non-dystrophic myopathy Non-hereditary degenerative ataxia Non-progressive cerebellar[] […] infantile neurologic onset Niemann-Pick disease type C, severe early infantile neurologic onset Niemann-Pick disease type C, severe perinatal form Nodular neuronal heterotopia Non-X-linked[]

  • Nemaline Myopathy

    myopathy rod myopathy nemaline body disease NEM NM edit English nemaline myopathy congenital structural myopathy characterized by generally non-progressive muscle weakness[] . : A follow-up study of congenital non-progressive myopathies. Brain Dev 1996 ; 18: 404 - 408.[] From Wikidata Jump to navigation Jump to search congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity nemaline rod[]

  • Hyaline Body Myopathy

    Hyaline body myopathy most likely represents a distinct congenital myopathy because of its childhoot-onset, non-progressive course, and distinct morphological features.[] Unlike the muscular dystrophies, the natural history of the congenital myopathies is typically non-progressive or very slowly progressive.[] Shy GM, Magee KR (1956) A new congenital non-progressive myopathy. Brain 79: 610–621 PubMed CrossRef Google Scholar 131.[]

  • Tubular Aggregate Myopathy

    Myotubular Myopathies, Congenital Structural Myopathies, X-Linked Centronuclear Myopathies, Congenital Non-Progressive Myopathy, Congenital Non Progressive Myopathies, Congenital[] Shy GM, Magee KR (1956) A new congenital non-progressive myopathy. Brain 79: 610–621 PubMed CrossRef Google Scholar 131.[] , X Linked Centronuclear Myopathy, Xlmtm, Myotubular Myopathies, Myotubular Myopathy 1, Myotubular Myopathy 1s, Centronuclear Myopathies, Tubular Aggregate Myopathies, X-Linked[]

  • Young Adult-Onset Distal Hereditary Motor Neuropathy

    […] aphasia Progressive supranuclear palsy - pure akinesia with gait freezing Blackfan-Diamond anemia Congenital myopathy with excess of thin filaments Dedifferentiated liposarcoma[] […] supranuclear palsy Progressive supranuclear palsy - corticobasal syndrome Progressive supranuclear palsy - parkinsonism Progressive supranuclear palsy - progressive non fluent[] […] deafness type DFNA Baraitser-Winter syndrome Adrenocortical carcinoma Li-Fraumeni syndrome Papilloma of choroid plexus Distal hereditary motor neuropathy type 2 Classical progressive[]

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