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46 Possible Causes for Spastic Paraplegia, Thenar Muscle Atrophy

  • Cervical Spondylosis

    […] groups, especially in the extremities poor or pathologic tandem gait atrophy of the hand’s thenar prominence (the fleshy fat pad just superior to the thumb on the ventral[americannursetoday.com] […] the following: clonus or spasticity of the lower extremities sensory changes (light touch, pinprick sensation, or temperature dysfunction) generalized weakness throughout muscle[americannursetoday.com]

  • Cervical Myelopathy

    paraplegia, normal pressure hydrocephalus, and spinal cord infarction can be easily differentiated on specific MRI findings.[boneandspine.com] […] groups, especially in the extremities poor or pathologic tandem gait atrophy of the hand’s thenar prominence (the fleshy fat pad just superior to the thumb on the ventral[americannursetoday.com] Other conditions like primary spinal cord tumors, syringomyelia, metastatic tumors, subacute combined degeneration of the spinal cord (vitamin B12 deficiency), hereditary spastic[boneandspine.com]

  • Cervical Herniated Disc

    For patients with more severe symptoms, such as spastic paresis and paraplegia, or those who fail conservative therapy, surgical treatment may be necessary.[symptoma.com]

  • Cervical Spinal Cord Tumor

    If you would like to participate in a clinical trial at Johns Hopkins, please go to the clinical trial database (ITCR), for more information. Study Title: NA_00023202 Principal Investigator: Chetan Bettagowda, MD Summary: Physicians at the Johns Hopkins Hospital are participating in a FDA approved clinical trial that is[…][hopkinsmedicine.org]

  • Autosomal Dominant Spastic Paraplegia Type 17

    MalaCards based summary : Spastic Paraplegia 17, also known as spastic paraplegia with amyotrophy of hands and feet, is related to spastic paraplegia 17, autosomal dominant[malacards.org] Homepage Rare diseases Search Search for a rare disease Autosomal dominant spastic paraplegia type 17 Disease definition A complex hereditary spastic paraplegia characterized[orpha.net] ORPHA:100998 Synonym(s): SPG17 Silver syndrome Spastic paraplegia-amyotrophy of hands and feet Prevalence: Inheritance: Autosomal dominant Age of onset: Childhood , Adolescent[orpha.net]

  • Distal Hereditary Motor Neuropathy Type 5

    Hmsn v refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see spastic paraplegia, hereditary).[icd10data.com] Novel syndromic form of X-linked complicated spastic paraplegia. Am J Med Genet 2000 ; 94 : 1 –4. Zatz M , Paula F, Starling A, Vainzof M.[jmg.bmj.com] Hereditary spastic paraplegia 3A associated with axonal neuropathy. JAMA Neurology, 64(5), 706-713.[sydney.edu.au]

  • Myelopathy

    Budka H, Sluga E, Heiss WD, Spastic Paraplegia Associated with Addisons-Disease - Adult Variant of Adreno-Leukodystrophy, J Neurol , 1976;213:237–50. 7.[touchneurology.com] […] groups, especially in the extremities poor or pathologic tandem gait atrophy of the hand’s thenar prominence (the fleshy fat pad just superior to the thumb on the ventral[americannursetoday.com] Positive findings on neurologic examination included a left afferent papillary defect, spastic paraplegia with hyperreflexia, crossed adductor responses, ankle clonus, and[jamanetwork.com]

  • Distal Myopathy Type 3

    paraplegia type 13 Autosomal dominant spastic paraplegia type 4 Autosomal recessive Emery-Dreifuss muscular dystrophy Autosomal recessive ataxia due to ubiquinone deficiency[csbg.cnb.csic.es] paraplegias, and hereditary sensory neuropathies.[mayomedicallaboratories.com] paraplegia Paget’s disease of bone 33 Epidemiology: Dutch family VCP mutation: Arg159Cys Clinical Onset Age: 5th to 6th decade Gait disorder Spastic paraparesis Tendon reflexes[neuromuscular.wustl.edu]

  • Spastic Paraplegia Type 38, Autosomal Dominant

    MalaCards based summary : Spastic Paraplegia 38, Autosomal Dominant, also known as spg38 , is related to spastic paraplegia 10 .[malacards.org] Genes and mapped phenotypes Gene ID: 100049707, updated on 8-Apr-2017 Summary Official Symbol SPG38 provided by HGNC Official Full Name spastic paraplegia 38 (autosomal dominant[ncbi.nlm.nih.gov] Synonym(s): spastic diplegia ; spastic paraplegia Erb-Duchenne paralysis - Synonym(s): Erb palsy[medical-dictionary.thefreedictionary.com]

  • Iatrogenic Cushing's Disease

    paraplegia Hereditary spherocytosis Herpes simplex encephalitis Herpes simplex virus infections Herpes virus infections Hiatal hernia Hip fractures Hirschsprung's disease[amboss.com] […] uremic syndrome Hemophilia Hemorrhoids Hemostasis and bleeding disorders Henoch-Schonlein purpura Hepatitis A Hepatitis B Hepatitis C Hepatocellular carcinoma Hereditary spastic[amboss.com]

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