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  1. 8 sty 2019 · Leukoencephalopathy with Axonal Spheroids and Pigmented Glia.—Studies (58–61) have shown that these pathologically defined entities are the result of autosomal dominant mutations in the colony-stimulating factor 1 receptor (CSF1R) gene. Both familial and de novo mutations have been described.

  2. Abstract. Adult-onset leukodystrophies and genetic leukoencephalopathies comprise a diverse group of neurodegenerative disorders of white matter with a wide age of onset and phenotypic spectrum. Patients with white matter abnormalities detected on MRI often present a diagnostic challenge to both general and specialist neurologists.

  3. 30 sty 2024 · Specific forms of white matter disease, such as MS or progressive multifocal leukoencephalopathy, may require other treatments. Those who have issues with balance and walking as a result of white...

  4. 22 lis 2019 · Given the success in preventing stroke in general, with important reductions in incidence and mortality, are new treatments to target cSVD progression even necessary? That they are is supported by the evidence that many patients with cSVD experience progression with cognitive and functional decline despite conventional stroke risk reduction.

  5. More than 100 heritable disorders can present with abnormal white matter on neuroimaging. While acquired disorders remain a more common cause of leukoencephalopathy in the adult than genetic causes, the clinician must remain aware of features that suggest a possible genetic etiology.

  6. Leukoencephalopathy (white matter disease) Damage to white matter may occur due to may conditions that can affect the brain. The clinical features, prognosis and treatment are related to the underlying condition.

  7. 17 sie 2021 · Since the characterization in the late 1990s of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, several other monogenic conditions leading to adult-onset ischemic or hemorrhagic stroke have been described.

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