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3,365 Possible Causes for Paraplegia, Persistent Notochordal Canal, Proximal Muscle Weakness Limb Girdle Distribution

  • Infantile-Onset Ascending Hereditary Spastic Paralysis

    Spastic paraplegia began during the first 2 years of life and extended to upper limbs within the next few years.[ncbi.nlm.nih.gov] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] All were considered normal at birth, and spastic paraplegia started approximately at the age of walking achievement.[ncbi.nlm.nih.gov]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • Meningomyelocele

    Clinical features include PARAPLEGIA, loss of sensation in the lower body, and incontinence.[connects.catalyst.harvard.edu] […] splits around that adhesion or persistence of the neurenteric canal, which would leave a connection of pluripotent cells between the ectoderm and the endoderm. [8] The role[asianjns.org] Neurological examination of the lower extremities showed paraplegia with hypotonia. Lesions were operated upon and closed by advancement flaps.[ingentaconnect.com]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • Infantile-Onset Autosomal Recessive Nonprogressive Cerebellar Ataxia

    […] nerve transmission giving rise to various clinical manifestations such as paresthesias, loss of vibratory sensation, and proprioception.Severe weakness, spasticity, clonus, paraplegia[explainmedicine.com] notochordal canal syndrome Salla disease Salt-and-pepper syndrome Sandhoff disease Sandhoff disease, adult form Sandhoff disease, infantile form Sandhoff disease, juvenile[se-atlas.de] Hereditary spastic paraplegia (HSP). See Hereditary Spastic Paraplegia Overview.[cmm.ucsd.edu]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • Lower Motor Neuron Syndrome with Late-Adult Onset

    […] spastic paraplegia type 41 Autosomal dominant spastic paraplegia type 42 Autosomal dominant spastic paraplegia type 6 Autosomal dominant spastic paraplegia type 8 Autosomal[se-atlas.de] Spastic paraplegia 17 (SPG17) is caused by mutations in the seipin gene on chromosome 11q12-q14.[clinicalgate.com] Hereditary Spastic Paraplegia Hereditary spastic paraplegia, also known as familial spastic paraparesis, consists of a diverse group of genetic disorders characterized by[neupsykey.com]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • X-linked Distal Spinal Muscular Atrophy Type 3

    ) • Progressive atrophy of humero-peroneal distribution (proximal muscles of upper limb and distal muscles of lower limb).[physio-pedia.com] 17, Autosomal Dominant Silver Spastic Paraplegia Syndrome Silver Syndrome Spastic Paraplegia 17 Spastic Paraplegia With Amyotrophy Of Hands And Feet SPG17 270685 Genetic[ukgtn.nhs.uk] […] agammaglobulinemia Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation Autosomal dominant Charcot-Marie-Tooth disease type 2F Autosomal dominant spastic paraplegia[csbg.cnb.csic.es]

    Missing: Persistent Notochordal Canal
  • Distal Hereditary Motor Neuropathy Type 1

    […] spastic paraplegia type 41 Autosomal dominant spastic paraplegia type 42 Autosomal dominant spastic paraplegia type 6 Autosomal dominant spastic paraplegia type 8 Autosomal[se-atlas.de] See also [ edit ] Motor neuron disease Hereditary motor and sensory neuropathies Spinal muscular atrophies Charcot–Marie–Tooth disease Hereditary spastic paraplegia References[en.wikipedia.org] […] syndrome, Spastic paraplegia 17 AR 34 50 CHCHD10 Myopathy, isolated mitochondrial, Frontotemporal dementia and/or amyotrophic lateral sclerosis 2, Spinal muscular atrophy[blueprintgenetics.com]

    Missing: Proximal Muscle Weakness Limb Girdle Distribution
  • Anterior Spinal Artery Syndrome

    A case of unexpected paraplegia after oesophageal resection under general anaesthesia combined with epidural analgesia and intra-operative intercostal block is described.[ncbi.nlm.nih.gov] METHODS: Eight patients were identified with spinal cord ischemia manifested by paraplegia or paraparesis after 1331 abdominal aortic operations.[ncbi.nlm.nih.gov] A 51-year-old woman with a history of breast cancer developed pulmonary edema and lower extremity paraplegia with preservation of proprioception as the initial manifestation[ncbi.nlm.nih.gov]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Carcinoma of the Prostate

    […] disease presents with inappetence and weight loss or with clinical manifestations related to bone metastases (pain and pathological fractures), spinal cord compression (paraplegia[symptoma.com] Treatment and prognosis of patients with paraplegia or quadriplegia because of metastatic spinal cord compression in prostate cancer.[ncbi.nlm.nih.gov]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Non-Hodgkin Lymphoma

    There are many different types of non-Hodgkin lymphoma (NHL). Doctors also give NHL a grade, depending on how quickly it is likely to grow. Low grade NHL Find out about low grade non-Hodgkin lymphoma (NHL), what low grade means, and different types. High grade NHL Find out about high grade lymphomas, what high[…][cancerresearchuk.org]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution
  • Radiculomyelopathy

    Paraplegia 32:627-30.[fluoridealert.org] Patient had paraplegia due to tuberculomas in the thoracic spinal cord.[nature.com] Paraplegia 28:244-51.[fluoridealert.org]

    Missing: Persistent Notochordal Canal Proximal Muscle Weakness Limb Girdle Distribution

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