Recurrent Dysarthria and Ataxia in a Young Girl

被引：0
作者：
Romba, Meghan [1 ]
Gonzalez-Giraldo, Ernesto [1 ]
Levy, Michael [1 ]
机构：
[1] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
来源：
JAMA NEUROLOGY | 2018年 / 75卷 / 01期
基金：
美国国家卫生研究院;
关键词：
MOG ANTIBODY; DISORDERS; DISEASE; NMO;
D O I：
10.1001/jamaneurol.2017.3085
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：125 / 126
页数：2
相关论文
共 50 条
  • [1] Recurrent ataxia and dysarthria in myelin oligodendrocyte glycoprotein antibody-associated disorder
    Chakraborty, Uddalak
    Ghosh, Shrestha
    Dana, Amlan Kusum
    Chandra, Atanu
    BMJ CASE REPORTS, 2021, 14 (11)
  • [2] The scale for the assessment and rating of ataxia correlates with dysarthria assessment in Friedreich's ataxia
    Eigentler, Andreas
    Rhomberg, Johanna
    Nachbauer, Wolfgang
    Ritzer, Irmgard
    Poewe, Werner
    Boesch, Sylvia
    JOURNAL OF NEUROLOGY, 2012, 259 (03) : 420 - 426
  • [3] Artificial Intelligence for Dysarthria Assessment in Children With Ataxia: A Hierarchical Approach
    Tartarisco, Gennaro
    Bruschetta, Roberta
    Summa, Susanna
    Ruta, Liliana
    Favetta, Martina
    Busa, Mario
    Romano, Alberto
    Castelli, Enrico
    Marino, Flavia
    Cerasa, Antonio
    Schirinzi, Tommaso
    Petrarca, Maurizio
    Bertini, Enrico
    Vasco, Gessica
    Pioggia, Giovanni
    IEEE ACCESS, 2021, 9 : 166720 - 166735
  • [4] Longitudinal change in dysarthria associated with Friedreich ataxia: a potential clinical endpoint
    Rosen, Kristin M.
    Folker, Joanne E.
    Vogel, Adam P.
    Corben, Louise A.
    Murdoch, Bruce E.
    Delatycki, Martin B.
    JOURNAL OF NEUROLOGY, 2012, 259 (11) : 2471 - 2477
  • [5] Mitochondrial DNA depletion and polg mutations in a patient with sensory ataxia, dysarthria and ophthalmoplegia
    Posada, Ignacio J.
    Esther Gallardo, Maria
    Dominguez, Cristina
    Rivera, Henry
    Cabello, Ana
    Arenas, Joaquin
    Martin, Miguel A.
    Garesse, Rafael
    Bornstein, Belen
    MEDICINA CLINICA, 2010, 135 (10): : 452 - 455
  • [6] Hyperpigmented atrophic lesions in a young girl
    Wu, Jessica
    Ma, Janice E.
    Smogorzewski, Jan
    PEDIATRIC DERMATOLOGY, 2020, 37 (06) : E85 - E86
  • [7] Preceding polydipsia/polyuria, ataxia, and dysarthria in an adult with mixed histiocytosis (Erdheim Chester disease/Langerhans cell histiocytosis)
    Miyoshi, Takashi
    Tamaki, Shigehisa
    Kudo, Ko
    Kono, Fumihiko
    Masada, Tomoya
    Imashuku, Shinsaku
    ANNALS OF HEMATOLOGY, 2022, 101 (12) : 2803 - 2804
  • [8] Detection and differentiation of ataxic and hypokinetic dysarthria in cerebellar ataxia and parkinsonian disorders via wave splitting and integrating neural networks
    Song, Joomee
    Lee, Ju Hwan
    Choi, Jungeun
    Suh, Mee Kyung
    Chung, Myung Jin
    Kim, Young Hun
    Park, Jeongho
    Choo, Seung Ho
    Son, Ji Hyun
    Lee, Dong Yeong
    Ahn, Jong Hyeon
    Youn, Jinyoung
    Kim, Kyung-Su
    Cho, Jin Whan
    PLOS ONE, 2022, 17 (06):
  • [9] A 2-year-old girl with a recurrent vesicular rash
    Paul, Mary K.
    Chang, Christopher
    ALLERGY AND ASTHMA PROCEEDINGS, 2014, 35 (04) : 349 - 352
  • [10] Tonsillar and Adenoid Noncaseating, Epithelioid Granulomas in a Young Girl
    Battat, Nir
    Tamir, Sharon Ovnat
    Marom, Tal
    JOURNAL OF CRANIOFACIAL SURGERY, 2019, 30 (06) : E508 - E511
12345