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144 Possible Causes for MRI Scan showing White Matter Lesions, Prominent High Nasal Root

  • Woodhouse Sakati Syndrome

    nasal bridge Elevated nasal bridge High nasal bridge Prominent bridge of nose Prominent nasal root Protruding bridge of nose Protruding nasal bridge [ more ] 0000426 Prominent[rarediseases.info.nih.gov] […] forehead, flattened occiput, triangular face, prominent nasal root, hypertelorism, downward slanting palpebral fissures), scoliosis, hyperreflexia and camptodactyly.[sites.uclouvain.be] […] forehead, flat occiput, triangular face, prominent nasal root, hypertelorism, and down-slanting palpebral fissures), scoliosis, hyperreflexia, and camptodactyly.[rarediseases.info.nih.gov]

  • Fabry Disease

    Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body including the kidneys, heart, and skin. Marchesoni, Cintia L.; Roa, Norma; Pardal, Ana María; Neumann, Pablo; Cáceres, Guillermo; Martínez, Pablo; Kisinovsky, Isaac; Bianchi, Silvia; Tarabuso, Ana Lía;[…][en.wikipedia.org]

    Missing: Prominent High Nasal Root
  • Lyme Meningoencephalitis

    Although Lyme disease frequently attacks the central nervous system, this involvement is rarely severe, and high-dose intravenous penicillin usually is adequate treatment. The patient we describe developed severe Lyme meningoencephalitis despite receiving a full course of penicillin, and his condition continued to[…][ncbi.nlm.nih.gov]

    Missing: Prominent High Nasal Root
  • Leigh's Disease

    Leigh syndrome (also called Leigh disease and subacute necrotizing encephalomyelopathy ) is an under-recognized inherited neurometabolic disorder that affects the central nervous system. It is named after Archibald Denis Leigh, a British neuropsychiatrist who first described the condition in 1951. [2] Normal levels[…][en.wikipedia.org]

    Missing: Prominent High Nasal Root
  • Alexander Disease

    Alexander disease is one of a group of neurological conditions known as the leukodystrophies, which are ailments caused by anomalies in the myelin, which protects nerve fibers in the brain. According to the National Institute of Neurological Disorders and Stroke, the destruction of white matter is accompanied by the[…][en.wikipedia.org]

    Missing: Prominent High Nasal Root
  • Diffuse Cerebral Sclerosis of Schilder

    Repeat MRI brain scan showed near-complete resolution of white matter edema, reduction in the size of the primary lesion with increased central cystic degeneration and surrounding[jmgims.co.in] Noncontrast computed tomography scan brain done in emergency showed a large area of white matter hypodensity involving the left frontoparietal region.[jmgims.co.in] Brain magnetic resonance imaging (MRI) showed an ill-defined lesion measuring 7.5 cm 4.4 cm 6.5 cm in the left centrum semiovale which was isointense on T1-weighted, hyperintense[jmgims.co.in]

    Missing: Prominent High Nasal Root
  • Progressive Multifocal Leukoencephalopathy

    show hypointense lesions within the affected white matter of patients with PML MRI demonstrates hyperintense lesions on T2 and FLAIR weighted images Faint, typically peripheral[pathologyoutlines.com] CT scan may show hypodense lesions.[emedicine.com] […] virus is the most useful laboratory diagnostic test but is not 100% sensitive (see above, J Clin Virol 2008;43:247, J Med Microbiol 2009;58:253 ) Radiology description CT scans[pathologyoutlines.com]

    Missing: Prominent High Nasal Root
  • Central Pontine Myelinolysis

    We use cookies to improve our service and to tailor our content and advertising to you. More info Close You can manage your cookie settings via your browser at any time. To learn more about how we use cookies, please see our cookies policy Close Intended for healthcare professionals Research Wernicke's...[…][doi.org]

    Missing: Prominent High Nasal Root
  • Metachromatic Leukodystrophy

    Metachromatic leukodystrophy is an autosomal recessive lysosomal storage disease consisting of progressive demyelination of the peripheral and central nervous systems. In most patients, it is attributed to a mutation in the arylsulfatase A (ARSA) gene, which in turn hinders the production of arysulfatase A. This[…][symptoma.com]

    Missing: Prominent High Nasal Root
  • Globoid Cell Leukodystrophy

    Globoid cell leukodystrophy is a rare, degenerative disease associated with progressive demyelination; symptom onset typically occurs in infancy. Globoid cell leukodystrophy may also be referred to as Krabbe disease. Patients suffering from type 1 GLC generally present during the first six months of their life.[…][symptoma.com]

    Missing: Prominent High Nasal Root

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