Bilateral hypertrophic olivary degeneration in genetic neurological disorders
- Authors: Suslin A.S.1, Seliverstov Y.A.1, Kremneva E.I.1, Krotenkova M.V.1
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Affiliations:
- Research Center of Neurology
- Issue: Vol 14, No 3 (2020)
- Pages: 81-87
- Section: Clinical analysis
- Submitted: 14.09.2020
- Published: 14.09.2020
- URL: https://annaly-nevrologii.com/journal/pathID/article/view/688
- DOI: https://doi.org/10.25692/ACEN.2020.3.11
- ID: 688
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Full Text
Abstract
Hypertrophic olivary degeneration (HOD) is a rare variant of transsynaptic degeneration in the inferior olivary nuclei due to a lesion within the dentato-rubro- olivary pathway, also known as the Guillain–Mollaret triangle. Bilateral HOD can be identified on MRI in patients with not only acquired but also genetic neurological disorders. The article describes patients with both common and rare genetic causes of the bilateral HOD. The pathophysiology of HOD is also briefly reviewed.
About the authors
Aleksander S. Suslin
Research Center of Neurology
Author for correspondence.
Email: suslin@neuroradiology.ru
Россия, Moscow
Yury A. Seliverstov
Research Center of Neurology
Email: suslin@neuroradiology.ru
Россия, Moscow
Elena I. Kremneva
Research Center of Neurology
Email: suslin@neuroradiology.ru
Россия, Moscow
Marina V. Krotenkova
Research Center of Neurology
Email: suslin@neuroradiology.ru
Россия, Moscow
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