Cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS) with chronic cough and preserved muscle stretch reflexes: evidence for selective sparing of afferent Ia fibres

被引:50
作者
Infante, Jon [1 ,2 ]
Garcia, Antonio [2 ,3 ]
Serrano-Cardenas, Karla M. [1 ,2 ]
Gonzalez-Aguado, Rocio [4 ]
Gazulla, Jos [5 ]
de Lucas, Enrique M. [6 ]
Berciano, Jos [1 ,2 ,7 ]
机构
[1] Univ Cantabria, Univ Hosp Marques Valdecilla IDIVAL, Serv Neurol, Santander, Spain
[2] Ctr Invest Biomed Red Enfermedades Neurodegenerat, Santander, Spain
[3] Univ Hosp Marques Valdecilla IDIVAL, Serv Clin Neurophysiol, Santander, Spain
[4] Univ Hosp Marques Valdecilla, Serv Otolaryngol, Santander, Spain
[5] Hosp Univ Miguel Servet, Serv Neurol, Zaragoza, Spain
[6] Univ Hosp Marques Valdecilla, Serv Radiol, Santander, Spain
[7] Univ Cantabria, Edificio Escuela Univ Enfermeria Carta Planta, Dept Med & Psychiat, Avda Valdecilla S-N, Santander 39008, Spain
关键词
Autosomal recessive inheritance; CANVAS; Cerebellar ataxia; Electrophysiology; Friedreich ataxia; Head impulse test; Hereditary sensory and autonomic neuropathy; Hypopallesthesia; Magnetic resonance imaging; Masseter reflex; Muscle spindle afferents (Ia fibres); Muscle stretch reflexes; OMIM; Riley-day syndrome; Rombergism; Sensory ganglionopathy; Sensory nerve action potentials; Somatosensory evoked potentials; Spasmodic cough; Sympathetic skin responses; T-reflex; Vestibular function testing; Vestibulo-ocular reflex; DISEASE TYPE 1A; SENSORY NEUROPATHY; BILATERAL VESTIBULOPATHY; AUTONOMIC DYSFUNCTION; DIAGNOSTIC-CRITERIA; FRIEDREICHS-ATAXIA; CLINICAL-FEATURES; MASSETER REFLEX; NEURONOPATHY; TYPE-2;
D O I
10.1007/s00415-018-8872-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of this study was to describe five patients with cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) with chronic cough and preserved limb muscle stretch reflexes. All five patients were in the seventh decade of age, their gait imbalance having been initiated in the fifth decade. In four patients cough antedated gait imbalance between 15 and 29 years; cough was spasmodic and triggered by variable factors. Established clinical picture included severe hypopallesthesia predominating in the lower limbs with postural imbalance, and variable degree of cerebellar axial and appendicular ataxia, dysarthria and horizontal gaze-evoked nystagmus. Upper- and lower-limb tendon jerks were preserved, whereas jaw jerk was absent. Vestibular function testing showed bilateral impairment of the vestibulo-ocular reflex. Nerve conduction studies demonstrated normal motor conduction parameters and absence or severe attenuation of sensory nerve action potentials. Somatosensory evoked potentials were absent or severely attenuated. Biceps and femoral T-reflex recordings were normal, while masseter reflex was absent or attenuated. Sympathetic skin responses were normal. Cranial MRI showed vermian and hemispheric cerebellar atrophy predominating in lobules VI, VII and VIIa. We conclude that spasmodic cough may be an integral part of the clinical picture in CANVAS, antedating the appearance of imbalance in several decades and that sparing of muscle spindle afferents (Ia fibres) is probably the pathophysiological basis of normoreflexia.
引用
收藏
页码:1454 / 1462
页数:9
相关论文
共 32 条
[1]   Brainstem reflexes: Electrodiagnostic techniques, physiology, normative data, and clinical applications [J].
Aramideh, M ;
De Visser, BWO .
MUSCLE & NERVE, 2002, 26 (01) :14-30
[2]   PRESERVATION OF THE MASSETER REFLEX IN FRIEDREICH ATAXIA [J].
AUGER, RG .
NEUROLOGY, 1992, 42 (04) :875-878
[3]   Chronic cough due to Thr124Met mutation in the peripheral myelin protein zero (MPZ gene) [J].
Baloh, RH ;
Jen, JC ;
Kim, G ;
Baloh, RW .
NEUROLOGY, 2004, 62 (10) :1905-1906
[4]   Charcot-Marie-Tooth disease type 1A duplication with severe paresis of the proximal lower limb muscles:: a long-term follow-up study [J].
Berciano, J. ;
Gallardo, E. ;
Garcia, A. ;
Infante, J. ;
Mateo, I. ;
Combarros, O. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2006, 77 (10) :1169-1176
[5]   Friedreich ataxia with minimal GAA expansion presenting as adult-onset spastic ataxia [J].
Berciano, J ;
Mateo, I ;
De Pablos, C ;
Polo, JM ;
Combarros, O .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2002, 194 (01) :75-82
[6]   FRIEDREICHS ATAXIA IN THE SOUTH OF ITALY - A CLINICAL AND BIOCHEMICAL SURVEY OF 23 PATIENTS [J].
CAMPANELLA, G ;
FILLA, A ;
DEFALCO, F ;
MANSI, D ;
DURIVAGE, A ;
BARBEAU, A .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1980, 7 (04) :351-357
[7]  
Carpenter MB, 1976, HUMAN NEUROANATOMY, P399
[8]  
Chiappa K. H., 1997, EVOKED POTENTIALS CL
[9]   Cerebellar ataxia with spasmodic cough -: A new form of dominant ataxia [J].
Coutinho, P ;
Cruz, VT ;
Tuna, A ;
Silva, SE ;
Guimaräes, J .
ARCHIVES OF NEUROLOGY, 2006, 63 (04) :553-555
[10]   Charcot-Marie-Tooth disease type 1A with 17p duplication in infancy and early childhood -: A longitudinal clinical and electrophysiologic study [J].
García, A ;
Combarros, O ;
Calleja, J ;
Berciano, J .
NEUROLOGY, 1998, 50 (04) :1061-1067