Early Onset Nonprogressive Generalized Dystonia Is Caused by Biallelic SHQ1 Variants

被引:0
|
作者
Revert Barbera, Anna [1 ]
Fernandez Isern, Guerau [2 ]
Dario Ortigoza-Escobar, Juan [3 ,4 ,5 ]
机构
[1] Hosp Mar Parc Salut Mar, Dept Neurol, Barcelona, Spain
[2] Inst Recerca Sant Joan Deu, Dept Genet & Mol Med IPER, Barcelona, Spain
[3] Inst Salud Carlos III, U 703 Ctr Biomed Res Rare Dis CIBER ER, Barcelona, Spain
[4] Hosp Sant Joan Deu Barcelona, Inst Recerca, Pediat Neurol Dept, Movement Disorders Unit, Barcelona, Spain
[5] European Reference Network Rare Neurol Dis ERN RN, Barcelona, Spain
关键词
D O I
10.1002/mds.29435
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:1118 / 1119
页数:3
相关论文
共 50 条
  • [21] TorsinA protein and neuropathology in early onset generalized dystonia with GAG deletion
    Rostasy, K
    Augood, SJ
    Hewett, JW
    Leung, JCO
    Sasaki, H
    Ozelius, LJ
    Ramesh, V
    Standaert, DG
    Breakefield, XO
    Hedreen, JC
    NEUROBIOLOGY OF DISEASE, 2003, 12 (01) : 11 - 24
  • [22] Biallelic Variants in UBAS Reveal that Disruption of the UFM1 Cascade Can Result in Early-Onset Encephalopathy
    Colin, Estelle
    Daniel, Jens
    Ziegler, Alban
    Wakim, Jamal
    Scrivo, Aurora
    Haack, Tobias B.
    Khiati, Salim
    Denomme, Anne-Sophie
    Amati-Bonneau, Patrizia
    Charif, Majida
    Procaccio, Vincent
    Reynier, Pascal
    Aleck, Kyrieckos A.
    Botto, Lorenzo D.
    Herper, Claudia Lena
    Kaiser, Charlotte Sophia
    Nabbout, Rima
    N'Guyen, Sylvie
    Antonio Mora-Lorca, Jose
    Assmann, Birgit
    Christ, Stine
    Meitinger, Thomas
    Strom, Tim M.
    Prokisch, Holger
    Miranda-Vizuete, Antonio
    Hoffmann, Georg F.
    Lenaers, Guy
    Bomont, Pascale
    Liebau, Eva
    Bonneau, Dominique
    AMERICAN JOURNAL OF HUMAN GENETICS, 2016, 99 (03) : 695 - 703
  • [23] Human SHQ1 variants R335C and A426V lead to severe ribosome biogenesis defects when expressed in yeast
    Alidou-D'Anjou, Ismael
    Patel, Aniket
    Sleiman, Sophie
    Dragon, Francois
    FRONTIERS IN GENETICS, 2023, 14
  • [24] Biallelic inheritance of hypomorphic PKD1 variants is highly prevalent in very early onset polycystic kidney disease
    Durkie, Miranda
    Chong, Jiehan
    Valluru, Manoj K.
    Harris, Peter C.
    Ong, Albert C. M.
    GENETICS IN MEDICINE, 2021, 23 (04) : 689 - 697
  • [25] Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism
    Joanne Leung
    Christine Klein
    Jennifer Friedman
    Peter Vieregge
    Helfried Jacobs
    Dana Doheny
    Christoph Kamm
    Deborah DeLeon
    Peter P. Pramstaller
    John B. Penney
    Marvin Eisengart
    Joseph Jankovic
    Thomas Gasser
    Susan B. Bressman
    David P. Corey
    Patricia Kramer
    Mitchell F. Brin
    Laurie J. Ozelius
    Xandra O. Breakefield
    Neurogenetics, 2001, 3 : 133 - 143
  • [26] Novel mutation in the TOR1A (DYT1) gene in atypical, early onset dystonia and polymorphisms in dystonia and early onset parkinsonism
    Leung, JC
    Klein, C
    Friedman, J
    Vieregge, P
    Jacobs, H
    Doheny, D
    Kamm, C
    DeLeon, D
    Pramstaller, PP
    Penney, JB
    Eisengart, M
    Jankovic, J
    Gasser, T
    Bressman, SB
    Corey, DP
    Kramer, P
    Brin, MF
    Ozelius, LJ
    Breakefield, XO
    NEUROGENETICS, 2001, 3 (03) : 133 - 143
  • [27] TOR1A sequence variants and the association with early-onset primary dystonia in the Chinese Han population
    Cheng, Fu Bo
    Wan, Xin Hua
    Zhang, Ying
    Miao, Jing
    Sun, Yuan
    Sun, Yan Bo
    Feng, Jia Chun
    PARKINSONISM & RELATED DISORDERS, 2013, 19 (03) : 399 - 401
  • [28] A rat knockin model of early onset DYT1 generalized dystonia displays abnormal hindlimb gait
    Frenz, C. T.
    Singh, M.
    Shashidharan, P.
    MOVEMENT DISORDERS, 2012, 27 : S340 - S340
  • [29] Biallelic CAV1 null variants induce congenital generalized lipodystrophy with achalasia
    Karhan, Asuman Nur
    Zammouri, Jamila
    Auclair, Martine
    Capel, Emilie
    Apaydin, Feramuz Demir
    Ates, Fehmi
    Verpont, Marie-Christine
    Magre, Jocelyne
    Feve, Bruno
    Lascols, Olivier
    Usta, Yusuf
    Jeru, Isabelle
    Vigouroux, Corinne
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2021, 185 (06) : 841 - 854
  • [30] TorsinA and DYT1 early-onset dystonia
    Kamm, Christoph
    Ozelius, Laurie J.
    Breakefield, Xandra O.
    FUTURE NEUROLOGY, 2008, 3 (01) : 61 - 72