Familial Spinocerebellar Ataxia Type 2 Parkinsonism Presenting as Intractable Oromandibular Dystonia

Kyung Ah Woo; Jee-Young Lee; Beomseok Jeon

doi:10.5334/tohm.506

Familial Spinocerebellar Ataxia Type 2 Parkinsonism Presenting as Intractable Oromandibular Dystonia

Tremor and Other Hyperkinetic Movements

Volume 9 (2019): Issue 0

By: Kyung Ah Woo, Jee-Young Lee and Beomseok Jeon

Open Access

|Feb 2019

Figures & Tables

Pedigree of the Spinocerebellar Ataxia Type 2 Korean Family. Adopted and revised from the pedigree in Kim et al.1 The red arrow indicates no. 32, the proband.

Structural and Functional Brain Imaging of the Patient. (A) Reduced dopamine transporter density in the anterior parts of both striata as shown in [¹⁸F]-FP-CIT positron emission tomography performed at age 59. (B,C) Brain magnetic resonance imaging at age 59 showed no definite cerebellar atrophy.

DOI: https://doi.org/10.5334/tohm.506 | Journal eISSN: 2160-8288

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Language: English

Submitted on: Oct 20, 2018

Accepted on: Dec 10, 2018

Published on: Feb 21, 2019

Published by: Columbia University Libraries/Information Services

In partnership with: Paradigm Publishing Services

Publication frequency: 1 issue per year

Keywords:

Dystonia,

spinocerebellar ataxia type 2,

Parkinson’s disease

© 2019 Kyung Ah Woo, Jee-Young Lee, Beomseok Jeon, published by Columbia University Libraries/Information Services
This work is licensed under the Creative Commons License.

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Familial Spinocerebellar Ataxia Type 2 Parkinsonism Presenting as Intractable Oromandibular Dystonia

Figures & Tables

Figure 1

Pedigree of the Spinocerebellar Ataxia Type 2 Korean Family. Adopted and revised from the pedigree in Kim et al.1 The red arrow indicates no. 32, the proband.

Figure 2

Structural and Functional Brain Imaging of the Patient. (A) Reduced dopamine transporter density in the anterior parts of both striata as shown in [¹⁸F]-FP-CIT positron emission tomography performed at age 59. (B,C) Brain magnetic resonance imaging at age 59 showed no definite cerebellar atrophy.

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Familial Spinocerebellar Ataxia Type 2 Parkinsonism Presenting as Intractable Oromandibular Dystonia

Figures & Tables

Figure 1

Pedigree of the Spinocerebellar Ataxia Type 2 Korean Family. Adopted and revised from the pedigree in Kim et al.1 The red arrow indicates no. 32, the proband.

Figure 2

Structural and Functional Brain Imaging of the Patient. (A) Reduced dopamine transporter density in the anterior parts of both striata as shown in [18F]-FP-CIT positron emission tomography performed at age 59. (B,C) Brain magnetic resonance imaging at age 59 showed no definite cerebellar atrophy.