Spinal muscular atrophy: Clinical classification and disease heterogeneity

被引:162
作者
Russman, Barry S.
机构
[1] Shriners Hosp Children, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97201 USA
关键词
spinal muscular atrophy; anterior horn cell; SMN1; gene;
D O I
10.1177/0883073807305673
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The clinical classification of spinal muscular atrophy, caused by deletion of the survival motor neuron I gene (SMNI), is based on age at onset and maximum function achieved. Evidence suggests that maximum function achieved is more closely related to life expectancy than age at onset. Therefore, it is important to wait for a period before assigning a patient to I of 5 classes of the disorder. Several diseases result from degeneration of the anterior horn cell but are not caused by SMN1. The classification for these conditions is evolving. This article offers an attempt at organizing one's thinking about this disease group.
引用
收藏
页码:946 / 951
页数:6
相关论文
共 50 条
  • [31] Therapeutic interventions for spinal muscular atrophy: preclinical and early clinical development opportunities
    Servais, Laurent
    Baranello, Giovanni
    Scoto, Mariacristina
    Daron, Aurore
    Oskoui, Maryam
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2021, 30 (05) : 519 - 527
  • [32] Intragenic and structural variation in the SMN locus and clinical variability in spinal muscular atrophy
    Wadman, Renske, I
    Jansen, Marc D.
    Stam, Marloes
    Wijngaarde, Camiel A.
    Curial, Chantall A. D.
    Medic, Jelena
    Sodaar, Peter
    Schouten, Jan
    Vijzelaar, Raymon
    Lemmink, Henny H.
    van den Berg, Leonard H.
    Groen, Ewout J. N.
    van der Pol, W. Ludo
    BRAIN COMMUNICATIONS, 2020, 2 (02)
  • [33] Analysis of spinal muscular atrophy patients from the spinal muscular atrophy and muscular dystrophy registry of Pakistan
    Aziz, Bisma
    Arif, Ahmed A.
    Kazi, Kulsum
    Kirmani, Salman
    Ansar, Zeeshan
    Nasir, Asghar
    Ibrahim, Shahnaz Hamid
    Ahmed, Khairunnisa Mukhtiar
    Hasan, Zahra
    Khan, Sara
    JOURNAL OF NEUROMUSCULAR DISEASES, 2025, 12 (02) : 260 - 270
  • [34] Spinal muscular atrophy: from animal model to clinical trial
    Zanoteli, Edmar
    Maximino, Jessica Ruivo
    Reed, Umbertina Conti
    Chadi, Gerson
    FUNCTIONAL NEUROLOGY, 2010, 25 (02) : 73 - 79
  • [35] Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy
    Maria C. Pera
    Giorgia Coratti
    Nicola Forcina
    Elena S. Mazzone
    Mariacristina Scoto
    Jacqueline Montes
    Amy Pasternak
    Anna Mayhew
    Sonia Messina
    Maria Sframeli
    Marion Main
    Robert Muni Lofra
    Tina Duong
    Danielle Ramsey
    Sally Dunaway
    Rachel Salazar
    Lavinia Fanelli
    Matthew Civitello
    Roberto de Sanctis
    Laura Antonaci
    Leonardo Lapenta
    Simona Lucibello
    Marika Pane
    John Day
    Basil T. Darras
    Darryl C. De Vivo
    Francesco Muntoni
    Richard Finkel
    Eugenio Mercuri
    BMC Neurology, 17
  • [36] RASCH ANALYSIS OF CLINICAL OUTCOME MEASURES IN SPINAL MUSCULAR ATROPHY
    Cano, Stefan J.
    Mayhew, Anna
    Glanzman, Allan M.
    Krosschell, Kristin J.
    Swoboda, Kathryn J.
    Main, Marion
    Steffensen, Birgit F.
    Berard, Carole
    Girardot, Francoise
    Payan, Christine A. M.
    Mercuri, Eugenio
    Mazzone, Elena
    Elsheikh, Bakri
    Florence, Julaine
    Hynan, Linda S.
    Iannaccone, Susan T.
    Nelson, Leslie L.
    Pandya, Shree
    Rose, Michael
    Scott, Charles
    Sadjadi, Reza
    Yore, Mackensie A.
    Joyce, Cynthia
    Kissel, John T.
    MUSCLE & NERVE, 2014, 49 (03) : 422 - 430
  • [37] Considerations for Treatment in Clinical Care of Spinal Muscular Atrophy Patients
    Voight, Stephanie
    Arya, Kapil
    CHILDREN-BASEL, 2024, 11 (04):
  • [38] Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy
    Pera, Maria C.
    Coratti, Giorgia
    Forcina, Nicola
    Mazzone, Elena S.
    Scoto, Mariacristina
    Montes, Jacqueline
    Pasternak, Amy
    Mayhew, Anna
    Messina, Sonia
    Sframeli, Maria
    Main, Marion
    Lofra, Robert Muni
    Duong, Tina
    Ramsey, Danielle
    Dunaway, Sally
    Salazar, Rachel
    Fanelli, Lavinia
    Civitello, Matthew
    de Sanctis, Roberto
    Antonaci, Laura
    Lapenta, Leonardo
    Lucibello, Simona
    Pane, Marika
    Day, John
    Darras, Basil T.
    De Vivo, Darryl C.
    Muntoni, Francesco
    Finkel, Richard
    Mercuri, Eugenio
    BMC NEUROLOGY, 2017, 17
  • [39] Spinal muscular atrophy: A changing phenotype beyond the clinical trials
    Tizzano, Eduardo F.
    Finkel, Richard S.
    NEUROMUSCULAR DISORDERS, 2017, 27 (10) : 883 - 889
  • [40] Clinical characteristics of three subtypes of spinal muscular atrophy in children
    Yuan, Ping
    Jiang, Li
    BRAIN & DEVELOPMENT, 2015, 37 (05) : 537 - 541