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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.
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页码:530 / 535
页数:6
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