Autosomal dominant congenital spinal muscular atrophy - A possible developmental deficiency of motor neurones?

被引:12
|
作者
Reddel, S. [1 ,2 ,4 ]
Ouvrier, R. A. [3 ,4 ]
Nicholson, G. [2 ,4 ]
Dierick, I. [5 ,6 ]
Irobi, J. [5 ,6 ]
Timmerman, V. [5 ,6 ]
Ryan, M. M. [7 ,8 ]
机构
[1] Concord Hosp, Dept Mol Med, Concord Repatriat Gen Hosp, Sydney, NSW 2139, Australia
[2] Concord Repatriat Gen Hosp, Dept Neurol, Sydney, NSW 2139, Australia
[3] Childrens Hosp Westmead, Inst Neuromuscular Res, Sydney, NSW, Australia
[4] Univ Sydney, Fac Med, Sydney, NSW 2006, Australia
[5] Univ Antwerp VIB, Dept Mol Genet, Peripheral Neuropathy Grp, B-2610 Antwerp, Belgium
[6] Univ Antwerp, Inst Born Bunge, Neurogenet Lab, Antwerp, Belgium
[7] Royal Childrens Hosp, Dept Neurosci, Parkville, Vic, Australia
[8] Murdoch Childrens Res Inst, Murdoch, WA, Australia
关键词
spinal muscular atrophy; dominant congenital spinal muscular atrophy; motor neuron disease; motor neuron apoptosis; arthrogryposis; talipes; electrophysiology; type I muscle fibre;
D O I
10.1016/j.nmd.2008.04.016
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We describe a kindred with an unusual congenital lower motor neuron disorder with significant but static muscle weakness predominantly affecting the lower limbs. The proband had talipes equinovarus and congenital hip contractures and did not walk until 19 months of age. Lower-extremity predominant, primarily proximal weakness was identified on assessment at three years. Over a 20 year follow-up there has been no clinical progression. The proband has a four-year-old daughter with very similar clinical findings. Electromyography and muscle biopsy suggest reduced numbers of giant normal duration motor units with little evidence of denervation or reinnervation. Dominant congenital spinal muscular atrophy predominantly affecting the lower limbs is rarely described. It is possible that the disorder is due to a congenital deficiency of motor neurons. Crown copyright (c) 2008 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:530 / 535
页数:6
相关论文
共 50 条
  • [21] SETX gene mutation in a family diagnosed autosomal dominant proximal spinal muscular atrophy
    Rudnik-Schoneborn, Sabine
    Arning, Larissa
    Epplen, Jorg T.
    Zerres, Klaus
    NEUROMUSCULAR DISORDERS, 2012, 22 (03) : 258 - 262
  • [22] Molecular Defects in the Motor Adaptor BICD2 Cause Proximal Spinal Muscular Atrophy with Autosomal-Dominant Inheritance
    Peeters, Kristien
    Litvinenko, Ivan
    Asselbergh, Bob
    Almeida-Souza, Leonardo
    Chamova, Teodora
    Geuens, Thomas
    Ydens, Elke
    Zimon, Magdalena
    Irobi, Joy
    De Vriendt, Els
    De Winter, Vicky
    Ooms, Tinne
    Timmerman, Vincent
    Tournev, Ivailo
    Jordanova, Albena
    AMERICAN JOURNAL OF HUMAN GENETICS, 2013, 92 (06) : 955 - 964
  • [23] The first Japanese family presenting as autosomal dominant proximal spinal muscular atrophy (OMIM 182980)
    Yamaguchi, K
    Uyama, E
    Hara, A
    Imamura, S
    Uchino, M
    ANNALS OF NEUROLOGY, 1998, 44 (03) : 473 - 473
  • [24] Vocal cord paralysis in autosomal dominant spinal muscular atrophy due to BICD2
    Matsui, Sachiko
    Iwatani, Sota
    Morisada, Naoya
    Takenouchi, Toshiki
    Yoshimoto, Seiji
    CONGENITAL ANOMALIES, 2023, 63 (02) : 52 - 53
  • [25] Autosomal-dominant proximal spinal muscular atrophy caused by mutations in a novel gene-motor adaptor BICD2
    Peeters, K.
    Litvinenko, I.
    Chamova, T.
    Asselbergh, B.
    Almeida-Souza, L.
    Geuens, T.
    Ydens, E.
    Zimon, M.
    Irobi, J.
    De Vriendt, E.
    De Winter, V.
    Ooms, T.
    Timmerman, V.
    Tournev, I.
    Jordanova, A.
    EUROPEAN JOURNAL OF NEUROLOGY, 2014, 21 : 94 - 94
  • [26] Autosomal-dominant proximal spinal muscular atrophy caused by mutations in a novel gene-motor adaptor BICD2
    Peeters, K.
    Litvinenko, I.
    Chamova, T.
    Asselbergh, B.
    Almeida-Souza, L.
    Geuens, T.
    Ydens, E.
    Zimon, M.
    Irobi, J.
    De Vriendt, E.
    De Winter, V.
    Ooms, T.
    Timmerman, V.
    Tournev, I.
    Jordanova, A.
    JOURNAL OF NEUROLOGY, 2014, 261 : S67 - S68
  • [27] THE MOTOR NEURON RESPONSE TO SMN1 DEFICIENCY IN SPINAL MUSCULAR ATROPHY
    Arnold, W. David
    Mo, Xiaokui
    Kolb, Stephen J.
    Burghes, Arthur H.
    Kissel, John T.
    MUSCLE & NERVE, 2014, 50 (03) : 457 - 458
  • [28] THE MOTOR NEURON RESPONSE TO SMN1 DEFICIENCY IN SPINAL MUSCULAR ATROPHY
    Kang, Peter B.
    Gooch, Clifton L.
    McDermott, Michael P.
    Darras, Basil T.
    Finkel, Richard S.
    Yang, Michele L.
    Sproule, Douglas M.
    Chung, Wendy K.
    Kaufmann, Petra
    de Vivo, Darryl C.
    MUSCLE & NERVE, 2014, 49 (05) : 636 - 644
  • [29] Congenital microvillus atrophy in a girl with autosomal dominant hypochondroplasia
    Heinz-Erian, P
    Schmidt, H
    Le Merrer, M
    Phillips, AD
    Kiess, W
    Hadorn, HB
    JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 1999, 28 (02): : 203 - 205
  • [30] AUTOSOMAL DOMINANT CONGENITAL ATROPHY OF OPTIC-NERVE
    ZOGRAFOS, L
    CUENDET, JF
    ANNALES D OCULISTIQUE, 1977, 210 (7-8): : 553 - 562