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72 Possible Causes for Segmental Spinal Muscular Atrophy

  • Monomelic Amyotrophy

    spinal muscular atrophy (JASSMA) — is an untreatable, focal motor neuron disease that primarily affects young (15–25 year old) males in India and Japan.[mmnforum.com] […] amyotrophy isn't especially common: Monomelic amyotrophy (MMA), also known as Hirayama disease, Sobue disease, juvenile non-progressive amyotrophy and juvenile asymmetric segmental[alsforums.com] . • Neurology,vol.72,number 24,june16,2009. 2. background • Hirayama disease (benign juvenile brachial spinal muscular atrophy, benign juvenile muscular atrophy of distal[slideshare.net]

  • Scoliosis

    […] dystrophies syringomyelia spinal dysraphism spinal muscular atrophy tethered cord infection resulting in bony abnormalities (e.g. pyogenic osteomyelitis , tuberculous spondylitis[radiopaedia.org] […] dystrophies syringomyelia spinal dysraphism spinal muscular atrophy tethered cord infection resulting in bony abnormalities (e.g. pyogenic osteomyelitis, tuberculous spondylitis[radiopaedia.org] Age of onset obviously varies with etiology, for example, spinal muscular atrophy produces deformity at a younger age than muscular dystrophy.[web.archive.org]

  • X-linked Distal Spinal Muscular Atrophy Type 3

    […] allelic with congenital distal spinal muscular atrophy and CMT2C Juvenile segmental spinal muscular atrophy (JSSMA) 183020 ?[ipfs.io] muscular atrophy in a small number of patients ( 5%).[blueprintgenetics.com] […] hypoplasia type 1A (PCH1A) 607596 VRK1 14q32 Autosomal dominant see Pontocerebellar hypoplasia MMA Juvenile asymmetric segmental spinal muscular atrophy (JASSMA) Monomelic[ipfs.io]

  • Adult Spinal Muscular Atrophy

    spinal muscular atrophy and juvenile asymmetric segmental spinal muscular atrophy.[symptoma.com] Differential diagnosis usually involves the other spinal muscle atrophies which include the X-linked spinal muscular atrophy, distal spinal muscular atrophy, autosomal dominant[symptoma.com]

  • Distal Spinal Muscular Atrophy Type 3

    […] allelic with congenital distal spinal muscular atrophy and CMT2C Juvenile segmental spinal muscular atrophy (JSSMA) 183020 ?[ipfs.io] […] hypoplasia type 1A (PCH1A) 607596 VRK1 14q32 Autosomal dominant see Pontocerebellar hypoplasia MMA Juvenile asymmetric segmental spinal muscular atrophy (JASSMA) Monomelic[ipfs.io] Characterised by severe muscle wasting as in SMA type I accompanied by congenital bone fractures PCH Spinal muscular atrophy with pontocerebellar hypoplasia (SMA-PCH) Pontocerebellar[ipfs.io]

  • Scapuloperoneal Spinal Muscular Atrophy

    […] allelic with congenital distal spinal muscular atrophy and CMT2C Juvenile segmental spinal muscular atrophy (JSSMA) 183020 ?[ipfs.io] 7q34–q36 Autosomal dominant Juvenile-onset Juvenile segmental spinal muscular atrophy (JSSMA) 183020 ? 18q21.3 ?[en.wikipedia.org] […] hypoplasia type 1A (PCH1A) 607596 VRK1 14q32 Autosomal dominant see Pontocerebellar hypoplasia MMA Juvenile asymmetric segmental spinal muscular atrophy (JASSMA) Monomelic[ipfs.io]

  • Upper Motor Neuron Disease

    […] bulbar palsy • Hexosaminidase deficiency • Multifocal motor neuropathies• Post polio syndrome • Post irradiation syndrome• Monomelic, focal or segmental spinal muscular atrophy[wiki.iop.kcl.ac.uk] Asymmetrical spinal muscular atrophy Occasionally patients present with asymmetrical, slowly progressive segmental weakness and wasting of the upper limb.[pn.bmj.com] Combined UMN and LMN involvement • Amyotrophic lateral sclerosis (ALS) Pure LMN involvement • Progressive Muscular Atrophy (PMA) • Proximal hereditary motor neuropathy• Hereditary[wiki.iop.kcl.ac.uk]

  • Lower Motor Neuron Syndrome with Late-Adult Onset

    […] distal spinal muscular atrophy (group 3a) and segmental proximal spinal muscular atrophy (group 3b).[ncbi.nlm.nih.gov] We propose to classify the patients in the different subgroups as slowly progressive spinal muscular atrophy (group 1), distal spinal muscular atrophy (group 2), segmental[ncbi.nlm.nih.gov]

  • Spinal Muscular Atrophy with Respiratory Distress Type 1

    Tülin Savaş, Ilknur Erol, Yasemin Özkale and Semra Saygi, Congenital Segmental Spinal Muscular Atrophy, Journal of Child Neurology, 10.1177/0883073814550497, 30, 4, (509-512[doi.org] Discussion Spinal muscular atrophies are autosomal recessive disorders that were previously classified according to clinical findings supported by neurophysiological examinations[tidsskriftet.no] It was previously shown that the three siblings had inherited the same DNA segments from their mother and father in the area of the IGHMBP2 gene.[tidsskriftet.no]

  • Spinal Muscular Atrophy Type 2

    7q34–q36 Autosomal dominant Juvenile-onset Juvenile segmental spinal muscular atrophy (JSSMA) 183020 ? 18q21.3 ?[en.wikipedia.org] Spine arthrodesis in patients with spinal muscular atrophy. J Bone Joint Surg A-64, 1982, 1179. Bowen JR, Forlin E. Spinal muscular atrophy. In: Weinstein SL, ed.[gait.aidi.udel.edu] (SMA-PCH) Pontocerebellar hypoplasia type 1A (PCH1A) 607596 VRK1 14q32 Autosomal dominant see Pontocerebellar hypoplasia MMA Juvenile asymmetric segmental spinal muscular[en.wikipedia.org]

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