Functionally Relevant Maculopathy and Optic Atrophy in Spinocerebellar Ataxia Type 1

BACKGROUND: Spinocerebellar ataxia type 1 (SCA‐ATXN1) is an inherited progressive ataxia disorder characterized by an adult‐onset cerebellar syndrome combined with nonataxia signs. Retinal or optic nerve affection are not systematically described. OBJECTIVES: To describe a retinal phenotype and its...

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Pubblicato in:Mov Disord Clin Pract
Autori principali: Oertel, Frederike Cosima, Zeitz, Oliver, Rönnefarth, Maria, Bereuter, Charlotte, Motamedi, Seyedamirhosein, Zimmermann, Hanna G., Kuchling, Joseph, Grosch, Anne Sophie, Doss, Sarah, Browne, Andrew, Paul, Friedemann, Schmitz‐Hübsch, Tanja, Brandt, Alexander U.
Natura: Artigo
Lingua:Inglês
Pubblicazione: John Wiley & Sons, Inc. 2020
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Research Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7328427/
https://ncbi.nlm.nih.gov/pubmed/32626794
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12949
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