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Posterior fossa involvement in the diagnosis of adult-onset inherited leukoencephalopathies

Abstract : Adult-onset genetic leukoencephalopathies are increasingly recognized. They are heterogeneous groups of disorders that commonly have distinct pathologic mechanisms but they share the presence of supratentorial bilateral and symmetric white matter hyperintensities. Although these abnormalities are usually non-specific, some specific MRI findings exist and sometimes help to distinguish these disorders. In this review, our aim is to describe posterior fossa abnormalities seen in the main adult-onset genetic leukoencephalopathies enabling clinicians to perform oriented genetic/metabolic screening.
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https://hal.umontpellier.fr/hal-01869107
Contributeur : Cécile Nowak <>
Soumis le : jeudi 6 septembre 2018 - 11:29:41
Dernière modification le : vendredi 15 mai 2020 - 12:22:06

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Xavier Ayrignac, Clemence Boutiere, Clarisse Carra-Dallière, Pierre Labauge. Posterior fossa involvement in the diagnosis of adult-onset inherited leukoencephalopathies. Journal of Neurology, Springer Verlag, 2016, 263 (12), pp.2361 - 2368. ⟨10.1007/s00415-016-8131-2⟩. ⟨hal-01869107⟩

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