Levodopa Responsive Dystonia Parkinsonism, Intellectual Disability, and Optic Atrophy Due to a Heterozygous Missense Variant in AFG3L2

被引:3
|
作者
Wong, Wui-Kwan [1 ,2 ]
Troedson, Christopher [1 ]
Dale, Russell C. [2 ]
Roscioli, Tony [3 ,4 ,5 ,6 ]
Field, Michael [7 ]
Palmer, Elizabeth [4 ,8 ]
Martin, Ellenore M. [9 ]
Kumar, Kishore R. [10 ,11 ,12 ]
Mohammad, Shekeeb S. [1 ,2 ]
机构
[1] Childrens Hosp Westmead, Nelson Dept Neurol & Neurosurg, Sydney, NSW, Australia
[2] Univ Sydney, Childrens Hosp, Westmead Clin Sch, Sydney Med,Sch Fac Med & Hlth, Westmead, NSW, Australia
[3] Prince Wales Hosp, Randwick Genom Lab, NSW Hlth Pathol, Sydney, NSW, Australia
[4] Sydney Childrens Hosp, Ctr Clin Genet, Randwick, NSW, Australia
[5] Univ New South Wales, Neurosci Res Australia NeuRA, Sydney, NSW, Australia
[6] Univ New South Wales, Prince Wales Clin Sch, Sydney, NSW, Australia
[7] Hunter Genet, Genet Learning Disabil GoLD Serv, Newcastle, NSW, Australia
[8] Univ New South Wales, Sch Womens & Childrens Hlth, Randwick, NSW, Australia
[9] Murdoch Childrens Res Inst, Brain & Mitochondria Res Grp, Melbourne, Vic, Australia
[10] Univ Sydney, Mol Med Lab, Concord Repatriat Gen Hosp, Concord Clin Sch, Sydney, NSW, Australia
[11] Univ Sydney, Neurol Dept, Concord Repatriat Gen Hosp, Concord Clin Sch, Sydney, NSW, Australia
[12] Garvan Inst Med Res, Kinghorn Ctr Clin Genom, Darlinghurst, NSW, Australia
来源
关键词
levodopa responsive dystonia-parkinsonism;
D O I
10.1002/mdc3.13538
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
[No abstract available]
引用
收藏
页码:S32 / S35
页数:4
相关论文
共 32 条
  • [21] Spastic ataxia and pseudo eye-of-the-tiger sign in a familiy with a novel compound heterozygous AFG3L2 mutations
    Calandra, C.
    Buda, G.
    Vishnopolska, S.
    Oliveri, J.
    Olivieri, F.
    Biagioli, G.
    Miquelini, L.
    Pellene, A.
    Marti, M.
    MOVEMENT DISORDERS, 2019, 34 : S167 - S168
  • [22] ATPase Domain AFG3L2 Mutations Alter OPA1 Processing and Cause Optic Neuropathy
    Caporali, Leonardo
    Magri, Stefania
    Legati, Andrea
    Del Dotto, Valentina
    Tagliavini, Francesca
    Balistreri, Francesca
    Nasca, Alessia
    La Morgia, Chiara
    Carbonelli, Michele
    Valentino, Maria L.
    Lamantea, Eleonora
    Baratta, Silvia
    Schoels, Ludger
    Schuele, Rebecca
    Barboni, Piero
    Cascavilla, Maria L.
    Maresca, Alessandra
    Capristo, Mariantonietta
    Ardissone, Anna
    Pareyson, Davide
    Cammarata, Gabriella
    Melzi, Lisa
    Zeviani, Massimo
    Peverelli, Lorenzo
    Lamperti, Costanza
    Marzoli, Stefania B.
    Fang, Mingyan
    Synofzik, Matthis
    Ghezzi, Daniele
    Carelli, Valerio
    Taroni, Franco
    ANNALS OF NEUROLOGY, 2020, 88 (01) : 18 - 32
  • [23] A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy
    Baderna, Valentina
    Schultz, Joshua
    Kearns, Lisa S.
    Fahey, Michael
    Thompson, Bryony A.
    Ruddle, Jonathan B.
    Huq, Aamira
    Maltecca, Francesca
    ACTA NEUROPATHOLOGICA COMMUNICATIONS, 2020, 8 (01)
  • [24] A novel AFG3L2 mutation close to AAA domain leads to aberrant OMA1 and OPA1 processing in a family with optic atrophy
    Valentina Baderna
    Joshua Schultz
    Lisa S. Kearns
    Michael Fahey
    Bryony A. Thompson
    Jonathan B. Ruddle
    Aamira Huq
    Francesca Maltecca
    Acta Neuropathologica Communications, 8
  • [25] A novel mutation located in the intermembrane space domain of AFG3L2 causes dominant optic atrophy through decreasing the stability of the encoded protein by ubiquitin-proteasome pathway
    Yang, Lin
    Xiuxiu, Jin
    Lei, Bo
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2022, 63 (07)
  • [26] Levodopa-Responsive Isolated Generalized Dystonia in a Patient with Alpha-Mannosidosis Due to a Novel Homozygous MAN2B1 Missense Variant-A Novel Association
    Holla, Vikram V.
    Gurram, Sandeep
    Kamath, Sneha D.
    Kamble, Nitish
    Yadav, Ravi
    Pal, Pramod Kumar
    MOVEMENT DISORDERS CLINICAL PRACTICE, 2024, 11 : S8 - S10
  • [27] Compound heterozygous mutation of AFG3L2 causes autosomal recessive spinocerebellar ataxia through mitochondrial impairment and MICU1 mediated Ca2+ overload
    Li, Hongyu
    Ma, Qingwen
    Xue, Yan
    Cai, Linlin
    Bao, Liwen
    Hong, Lei
    Zeng, Yitao
    Huang, Shu-Zhen
    Finnell, Richard H.
    Zeng, Fanyi
    SCIENCE CHINA-LIFE SCIENCES, 2025, 68 (02) : 484 - 501
  • [28] SPG7 Variant Escapes Phosphorylation-Regulated Processing by AFG3L2, Elevates Mitochondrial ROS, and Is Associated with Multiple Clinical Phenotypes
    Almontashiri, Naif A. M.
    Chen, Hsiao-Huei
    Mailloux, Ryan J.
    Tatsuta, Takashi
    Teng, Allen C. T.
    Mahmoud, Ahmad B.
    Ho, Tiffany
    Stewart, Nicolas A. S.
    Rippstein, Peter
    Harper, Mary Ellen
    Roberts, Robert
    Willenborg, Christina
    Erdmann, Jeanette
    Pastore, Annalisa
    McBride, Heidi M.
    Langer, Thomas
    Stewart, Alexandre F. R.
    CELL REPORTS, 2014, 7 (03): : 834 - 847
  • [29] SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy
    Kirsten Svenstrup
    Troels Tolstrup Nielsen
    Frederik Aidt
    Nina Rostgaard
    Morten Duno
    Flemming Wibrand
    Tua Vinther-Jensen
    Ian Law
    John Vissing
    Peter Roos
    Lena Elisabeth Hjermind
    Jørgen Erik Nielsen
    The Cerebellum, 2017, 16 : 62 - 67
  • [30] SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy
    Svenstrup, Kirsten
    Nielsen, Troels Tolstrup
    Aidt, Frederik
    Rostgaard, Nina
    Duno, Morten
    Wibrand, Flemming
    Vinther-Jensen, Tua
    Law, Ian
    Vissing, John
    Roos, Peter
    Hjermind, Lena Elisabeth
    Nielsen, Jorgen Erik
    CEREBELLUM, 2017, 16 (01): : 62 - 67