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
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
收藏
页码:136 / 140
页数:5
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