CLINICAL FEATURES AND FOLLOW-UP OF FOUR NEW CASES OF FACIAL-ONSET SENSORY AND MOTOR NEURONOPATHY

被引：24

作者：

Fluchere, Frederique ^{[2
]}

Verschueren, Annie ^{[1
]}

Cintas, Pascal ^{[3
]}

Franques, Jerome ^{[1
]}

Serratrice, Jacques ^{[4
]}

Weiller, Pierre J. ^{[4
]}

Azulay, Jean P. ^{[2
]}

Pouget, Jean ^{[1
]}

Attarian, Shahram ^{[1
]}

机构：

[1] CHU La Timone, Dept Neurol & Neuromuscular Dis, F-13385 Marseille 05, France

[2] CHU La Timone, Dept Neurol & Movement Disorders, F-13385 Marseille 05, France

[3] Hop Rangueil, Dept Neurol, Toulouse, France

[4] CHU La Timone, Dept Internal Med, F-13385 Marseille 05, France

来源：

MUSCLE & NERVE | 2011年 / 43卷 / 01期

关键词：

amyotrophic lateral sclerosis; bulbospinal muscle atrophy; FOSMN syndrome; motor neuronopathy; sensory neuronopathy; AMYOTROPHIC-LATERAL-SCLEROSIS; TANGIER-DISEASE; FOSMN SYNDROME; SPINAL-CORD; NEUROPATHY; PATHOLOGY; LYMPHOMA; ATROPHY;

D O I：

10.1002/mus.21884

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

In this study we report three patients with facial-onset sensory and motor neuronopathy (FOSMN), including the first female to be described. A fourth rather atypical case of a pyramidal syndrome with a fast rate of progression is also described. These cases raise the question as to whether upper motor neuron impairment is involved in FOSMN and whether there is a link between this syndrome and amyotrophic lateral sclerosis. The existence of this syndrome suggests that it may be wise to monitor all patients with isolated idiopathic trigeminal sensory neuropathy to ensure that this type of motor neuron disease is not overlooked. Muscle Nerve 43: 136-140, 2011

引用

页码：136 / 140

页数：5

共 17 条

[11] Amyotrophic lateral sclerosis with sensory neuropathy: part of a multisystem disorder?
Isaacs, Jeremy D.
Dean, Andrew F.
Shaw, Christopher E.
Al-Chalabi, Ammar
Mills, Kerry R.
Leigh, P. Nigel
[J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2007, 78 (07) : 750 - 753
[12] Sporadic bulbospinal muscle atrophy with facial-onset sensory neuropathy
Isoardo, Gianluca
Troni, Walter
[J]. MUSCLE & NERVE, 2008, 37 (05) : 659 - 662
[13] TRIGEMINAL SENSORY NEUROPATHY - A STUDY OF 22 CASES
LECKY, BRF
HUGHES, RAC
MURRAY, NMF
[J]. BRAIN, 1987, 110 : 1463 - 1485
[14] Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study
Pugdahl, K.
Fuglsang-Frederiksen, A.
de Carvalho, M.
Johnsen, B.
Fawcett, P. R. W.
Labarre-Vila, A.
Liguori, R.
Nix, W. A.
Schofield, I. S.
[J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2007, 78 (07) : 746 - 749
[15] Facial onset sensory and motor neuronopathy (FOSMN syndrome): a novel syndrome in neurology
Vucic, S.
Tian, D.
Chong, P. Siao Tick
Cudkowicz, M. E.
Hedley-Whyte, E. T.
Cros, D.
[J]. BRAIN, 2006, 129 : 3384 - 3390
[16] Sporadic motor neuron disease with severe sensory neuronopathy
Wakabayashi, K
Horikawa, Y
Oyake, M
Suzuki, S
Morita, T
Takahashi, H
[J]. ACTA NEUROPATHOLOGICA, 1998, 95 (04) : 426 - 430
[17] A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier disease
Züchner, S
Sperfeld, AD
Senderek, J
Sellhaus, B
Hanemann, CO
Schröder, JM
[J]. BRAIN, 2003, 126 : 920 - 927

← 1 2 →