Early recognition of SGCE-myoclonus-dystonia in children

被引:4
|
作者
Correa-Vela, Marta [1 ,2 ]
Carvalho, Joao [3 ]
Ferrero-Turrion, Julia [1 ]
Cazurro-Gutierrez, Ana [1 ]
Vanegas, Maria [1 ,4 ]
Gonzalez, Victoria [5 ]
Alvarez, Ramiro [6 ]
Marce-Grau, Anna [1 ]
Moreno, Antonio [2 ,7 ,8 ]
Macaya-Ruiz, Alfons [1 ,2 ,9 ]
Perez-Duenas, Belen [1 ,2 ,8 ,9 ]
机构
[1] Vall dHebron Hosp Univ, Dept Pediat Neurol, Pediat, Barcelona, Spain
[2] Univ Autonoma Barcelona, Dept Pediat, Barcelona, Spain
[3] Hosp Garcia Orta Almada, Ctr Desenvolvimento Crianca Torrado Silva, Pediat Neurol, Almada, Portugal
[4] Evelina Childrens Hosp, Paediat Dept, London, England
[5] Hosp Valle De Hebron, Dept Neurol, Barcelona, Spain
[6] Hosp Germans Trias, Dept Neurol, Barcelona, Spain
[7] Vall dHebron Barcelona Hosp Campus, Dept Pediat, Barcelona, Spain
[8] Inst Salud Carlos III ISCIII, CIBER Rare Dis CIBERER, Madrid, Spain
[9] Vall dHebron Res Inst, Neurol Res Grp, Barcelona, Spain
来源
关键词
EPSILON-SARCOGLYCAN MUTATIONS; FAMILY; GENE;
D O I
10.1111/dmcn.15298
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aim To evaluate early dystonic features in children and adolescents with SGCE-myoclonus-dystonia. Method In this cross-sectional study, 49 patients (26 females and 23 males) with SGCE-myoclonus-dystonia (aged 15y 2mo, SD 12y) with childhood-onset (2y 10mo, SD 1y 10mo) dystonia were examined using a standardized video recorded protocol. Dystonia was rated using the Writer's Cramp and Gait Dystonia Rating Scales. Disability and impairment for handwriting and walking were also rated. Results Dystonia was present at rest (n=1), posture (n=12), and during specific motor tasks (n=45) such as writing (n=35), walking (n=23), and running (n=20). Most children reported disability while performing these tasks. Early dystonic patterns were identified for writer's cramp and gait dystonia, the latter named the 'circular shaking leg', 'dragging leg', and 'hobby-horse gait' patterns. Sensory tricks were used by five and eight children to improve dystonia and myoclonus during writing and walking respectively. The rating scales accurately measured the severity of action dystonia and correlated with self-reported disability. Interpretation Children with SGCE-myoclonus-dystonia show recognizable dystonic patterns and sensory tricks that may lead to an early diagnosis and timely therapeutic approach. Isolated writer's cramp is a key feature in childhood and should prompt SCGE analysis. The proposed action dystonia scales could be used to monitor disease course and response to treatment.
引用
收藏
页码:207 / 214
页数:8
相关论文
共 50 条
  • [31] A novel mutation of the SGCE-gene in a German family with myoclonus-dystonia syndrome
    Christian Johannes Hartmann
    Barbara Leube
    Lars Wojtecki
    Beate Betz
    Stefan Jun Groiss
    Peter Bauer
    Alfons Schnitzler
    Martin Südmeyer
    Journal of Neurology, 2011, 258 : 1186 - 1188
  • [32] KCTD17 is a confirmed new gene for dystonia, but is it responsible for SGCE-negative myoclonus-dystonia?
    Mencacci, Niccolo E.
    Brueggemann, Norbert
    PARKINSONISM & RELATED DISORDERS, 2019, 61 : 1 - 3
  • [33] A novel SGCE gene mutation in a Moroccan sporadic case with myoclonus-dystonia syndrome
    Rachad, Laila
    El Otmani, Hicham
    Karkar, Adnane
    El Kadmiri, Nadia
    Nadifi, Sellama
    GENE REPORTS, 2018, 11 : 121 - 123
  • [34] Pallidal deep brain stimulation for patients with myoclonus-dystonia without SGCE mutations
    Ikezawa, Jun
    Yokochi, Fusako
    Okiyama, Ryoichi
    Isoo, Ayako
    Agari, Takashi
    Kamiyama, Tsutomu
    Yugeta, Akihiro
    Tojima, Maya
    Kawasaki, Takashi
    Watanabe, Katsushige
    Kumada, Satoko
    Takahashi, Kazushi
    JOURNAL OF NEUROLOGY, 2024, 271 (06) : 2948 - 2954
  • [35] Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia
    Sperandeo, Alessandra
    Tamburini, Claudia
    Noakes, Zoe
    de la Fuente, Daniel Cabezas
    Keefe, Francesca
    Petter, Olena
    Plumbly, William
    Clifton, Nicholas E.
    Li, Meng
    Peall, Kathryn J.
    BRAIN, 2023, 146 (04) : 1523 - 1541
  • [36] Do distribution and co-existent myoclonus and dystonia aid in the identification of SGCE mutations?
    Zutt, R.
    Dijk, J. M.
    Peall, K.
    Speelman, H.
    Dreissen, Y. E. M.
    Contarino, M. F.
    Tijssen, M. A. J.
    MOVEMENT DISORDERS, 2015, 30 : S474 - S475
  • [37] Clinical and neurophysiological improvement of SGCE myoclonus-dystonia with GPi deep brain stimulation
    Kurtis, Monica M.
    San Luciano, Marta
    Yu, Qiping
    Goodman, Robert R.
    Ford, Blair
    Raymond, Deborah
    Pullman, Seth L.
    Saunders-Pullman, Rachel
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2010, 112 (02) : 149 - 152
  • [38] Novel and De Novo mutations of the SGCE gene in Brazilian patients with myoclonus-dystonia
    Borges, Vanderci
    de Carvalho Aguiar, Patricia
    Ferraz, Henrique Ballalai
    Ozelius, Laurie J.
    MOVEMENT DISORDERS, 2007, 22 (08) : 1208 - 1209
  • [39] Distribution and Coexistence of Myoclonus and Dystonia as Clinical Predictors of SGCE Mutation Status: A Pilot Study
    Zutt, Rodi
    Dijk, Joke M.
    Peall, Kathryn J.
    Speelman, Hans
    Dreissen, Yasmine E. M.
    Contarino, Maria Fiorella
    Tijssen, Marina A. J.
    FRONTIERS IN NEUROLOGY, 2016, 7
  • [40] SGCE isoform characterization and expression in human brain: implications for myoclonus-dystonia pathogenesis?
    Ritz, Katja
    van Schaik, Barbera D. C.
    Jakobs, Marja E.
    van Kampen, Antoine H.
    Aronica, Eleonora
    Tijssen, Marina A.
    Baas, Frank
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2011, 19 (04) : 438 - 444