Literature DB >> 36263189

Two Cases of Monozygotic Twins with Early-onset Isolated (DYT1) Dystonia Effectively Treated with Bilateral Globus Pallidus Internus Stimulation.

Yosuke Okazaki1, Tatsuya Sasaki1, Kouji Kawai1, Kakeru Hosomoto1, Susumu Sasada1, Takao Yasuhara1, Tomoyuki Akiyama2, Yoshiyuki Hanaoka3, Isao Date1.   

Abstract

Early-onset isolated (DYT1) dystonia is one of the most common forms of primary dystonia in childhood, and deep brain stimulation of the globus pallidus internus (GPi-DBS) is a highly effective treatment for it. However, the effectiveness of GPi-DBS in monozygotic twins with DYT1 dystonia has never been reported globally. Here, we report the cases of monozygotic twins with DYT1 dystonia who were treated using GPi-DBS, and we include a literature review. The younger brother showed an abnormal gait, with external rotation of the right lower leg at 6 years old. The symptoms gradually became so severe that he had difficulty walking on his own at 9 years of age. Treatment with levodopa-carbidopa partially resolved his symptoms, but most of the symptoms remained. Meanwhile, the older brother developed dystonia in both upper limbs at 8 years of age, with gradual symptom progression. At 13 years of age, they were diagnosed with DYT1 dystonia. Bilateral GPi-DBS was performed in both patients at 16 years of age. Their symptoms remarkably improved after surgery. The Burke-Fahn-Marsden dystonia rating scale (BFMDRS) movement score was reduced from 52 to 2 points for the younger brother and from 35 to 1 point for the older brother. Even if monozygotic twins have the same genes, the onset and severity of symptoms might vary in accordance with differences in epigenomic profiles. However, GPi-DBS treatment was very effective for the two cases; thus, we should consider the surgical interventions for each patient.
© 2022 The Japan Neurosurgical Society.

Entities:  

Keywords:  DYT1 dystonia; deep brain stimulation of the globus pallidus internus; monozygotic twins

Year:  2022        PMID: 36263189      PMCID: PMC9534566          DOI: 10.2176/jns-nmc.2022-0084

Source DB:  PubMed          Journal:  NMC Case Rep J        ISSN: 2188-4226


  22 in total

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Journal:  Neurology       Date:  2003-01-28       Impact factor: 9.910

2.  Segregation analysis of idiopathic torsion dystonia in Ashkenazi Jews suggests autosomal dominant inheritance.

Authors:  N J Risch; S B Bressman; D deLeon; M F Brin; R E Burke; P E Greene; H Shale; E B Claus; L A Cupples; S Fahn
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

3.  Marked improvement in Segawa syndrome after L-dopa and selegiline treatment.

Authors:  Elif Yosunkaya; Ender Karaca; Sarenur Basaran; Mehmet Seven; Adnan Yüksel
Journal:  Pediatr Neurol       Date:  2010-05       Impact factor: 3.372

4.  Intrafamilial phenotypic variability of the DYT1 dystonia: from asymptomatic TOR1A gene carrier status to dystonic storm.

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Journal:  Mov Disord       Date:  2002-03       Impact factor: 10.338

5.  Pallidal deep-brain stimulation in primary generalized or segmental dystonia.

Authors:  Andreas Kupsch; Reiner Benecke; Jörg Müller; Thomas Trottenberg; Gerd-Helge Schneider; Werner Poewe; Wilhelm Eisner; Alexander Wolters; Jan-Uwe Müller; Günther Deuschl; Marcus O Pinsker; Inger Marie Skogseid; Geir Ketil Roeste; Juliane Vollmer-Haase; Angela Brentrup; Martin Krause; Volker Tronnier; Alfons Schnitzler; Jürgen Voges; Guido Nikkhah; Jan Vesper; Markus Naumann; Jens Volkmann
Journal:  N Engl J Med       Date:  2006-11-09       Impact factor: 91.245

Review 6.  Emerging concepts in the physiological basis of dystonia.

Authors:  Angelo Quartarone; Mark Hallett
Journal:  Mov Disord       Date:  2013-06-15       Impact factor: 10.338

7.  Myoclonus-dystonia and spinocerebellar ataxia type 14 presenting with similar phenotypes: trunk tremor, myoclonus, and dystonia.

Authors:  Elisabeth M J Foncke; Richard J Beukers; Cees C Tijssen; Johannes H T M Koelman; Marina A J Tijssen
Journal:  Parkinsonism Relat Disord       Date:  2009-11-12       Impact factor: 4.891

8.  PRRT2 mutation causes paroxysmal kinesigenic dyskinesia and hemiplegic migraine in monozygotic twins.

Authors:  Claudia Castiglioni; Isabel López; Florence Riant; Enrico Bertini; Alessandra Terracciano
Journal:  Eur J Paediatr Neurol       Date:  2012-11-19       Impact factor: 3.140

Review 9.  [Dystonia genes and elucidation of their roles in dystonia pathogenesis].

Authors:  Toshitaka Kawarai; Ryosuke Miyamoto; Nagahisa Murakami; Yoshimichi Miyazaki; Hidetaka Koizumi; Wataru Sako; Youhei Mukai; Kenta Sato; Shinichi Matsumoto; Takashi Sakamoto; Yuishin Izumi; Ryuji Kaji
Journal:  Rinsho Shinkeigaku       Date:  2013

10.  Monozygotic twins with DYT-TOR1A showing jerking movements and levodopa responsiveness.

Authors:  Yoshiyuki Hanaoka; Tomoyuki Akiyama; Harumi Yoshinaga; Ryousuke Miyamoto; Toshitaka Kawarai; Ryuji Kaji; Katsuhiro Kobayashi
Journal:  Brain Dev       Date:  2021-04-05       Impact factor: 1.961

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