Oral phase dysphagia in facial onset sensory and motor neuronopathy

Facial onset motor and sensory neuronopathy (FOSMN) is a rare disease whose cardinal features are initial asymmetrical facial sensory deficits followed by bulbar symptoms and spreading of sensory and motor deficits from face to scalp, neck, upper trunk, and upper extremities in a rostral–caudal direction. Although bulbar involvement is frequently observed in FOSMN, dysphagia in these patients has not been fully described. In this study, we aimed to characterize dysphagia as a prognostic factor in FOSMN by investigating our institutional case series.

[1]  C. Gerloff,et al.  Critical Dysphagia is Common in Parkinson Disease and Occurs Even in Early Stages: A Prospective Cohort Study , 2018, Dysphagia.

[2]  G. Sobue,et al.  Swallowing markers in spinal and bulbar muscular atrophy , 2017, Annals of clinical and translational neurology.

[3]  Qian Zheng,et al.  Facial onset sensory and motor neuronopathy , 2016, Neurological Sciences.

[4]  C. Gellera,et al.  Amyotrophic lateral sclerosis causes small fiber pathology , 2016, European journal of neurology.

[5]  P. Leigh,et al.  Recognising facial onset sensory motor neuronopathy syndrome: insight from six new cases , 2015, Practical Neurology.

[6]  J. Attems,et al.  Facial Onset Sensory and Motor Neuronopathy: Further Evidence for a TDP-43 Proteinopathy , 2015, Case Reports in Neurology.

[7]  L. Santoro,et al.  Differential trigeminal myelinated and unmyelinated nerve fiber involvement in FOSMN syndrome , 2015, Neurology.

[8]  A. Waldman,et al.  The Role of Functional Dopamine-Transporter SPECT Imaging in Parkinsonian Syndromes, Part 2 , 2015, American Journal of Neuroradiology.

[9]  A. Waldman,et al.  The Role of Functional Dopamine-Transporter SPECT Imaging in Parkinsonian Syndromes, Part 1 , 2015, American Journal of Neuroradiology.

[10]  G. Cruccu,et al.  Trigeminal isolated sensory neuropathy (TISN) and FOSMN syndrome: despite a dissimilar disease course do they share common pathophysiological mechanisms? , 2014, BMC Neurology.

[11]  I. Karakis,et al.  Facial onset sensory and motor neuronopathy (FOSMN) of childhood onset , 2014, Muscle & nerve.

[12]  G. Mora,et al.  Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis , 2014, Journal of Neurology, Neurosurgery & Psychiatry.

[13]  T. Iwaki,et al.  TAR DNA-binding protein 43 pathology in a case clinically diagnosed with facial-onset sensory and motor neuronopathy syndrome: An autopsied case report and a review of the literature , 2013, Journal of the Neurological Sciences.

[14]  S. V. Shanmugam,et al.  Facial onset sensory motor neuronopathy: an immunoglobulin-responsive case. , 2013, Journal of clinical neuromuscular disease.

[15]  P. Girlanda,et al.  Facial onset sensory motor neuronopathy: not always a slowly progressive disorder , 2013, Journal of Neurology.

[16]  L. Herbelin,et al.  Facial Onset Sensorimotor Neuronopathy Syndrome: A Case Series , 2012, Journal of clinical neuromuscular disease.

[17]  S. Tisch,et al.  FOSMN syndrome , 2012, Neurology.

[18]  A. Chiò,et al.  Phenotypic heterogeneity of amyotrophic lateral sclerosis: a population based study , 2011, Journal of Neurology, Neurosurgery & Psychiatry.

[19]  J. Pouget,et al.  Clinical features and follow‐up of four new cases of facial‐onset sensory and motor neuronopathy , 2011, Muscle & nerve.

[20]  政光 兵頭,et al.  嚥下内視鏡検査におけるスコア評価基準 (試案) の作成とその臨床的意義 , 2010 .

[21]  H. Shigeto,et al.  Facial onset sensory and motor neuronopathy (FOSMN) syndrome responding to immunotherapies , 2008, Journal of the Neurological Sciences.

[22]  W. Troni,et al.  Sporadic bulbospinal muscle atrophy with facial‐onset sensory neuropathy , 2008, Muscle & nerve.

[23]  M. Cudkowicz,et al.  Facial onset sensory and motor neuronopathy (FOSMN syndrome): a novel syndrome in neurology. , 2006, Brain : a journal of neurology.

[24]  R. Higo,et al.  Longitudinal analysis of progression of dysphagia in amyotrophic lateral sclerosis. , 2004, Auris, nasus, larynx.

[25]  S H Appel,et al.  Natural history of amyotrophic lateral sclerosis in a database population. Validation of a scoring system and a model for survival prediction. , 1995, Brain : a journal of neurology.

[26]  M. Hyodo,et al.  [New scoring proposed for endoscopic swallowing evaluation and clinical significance]. , 2010, Nihon Jibiinkoka Gakkai kaiho.

[27]  Ellen B. Roecker,et al.  A penetration-aspiration scale , 2004, Dysphagia.

[28]  N. Colodny.  Interjudge and Intrajudge Reliabilities in Fiberoptic Endoscopic Evaluation of Swallowing (Fees®) Using the Penetration–Aspiration Scale: A Replication Study , 2002, Dysphagia.

[29]  S. Langmore.  Endoscopic Evaluation and Treatment of Swallowing Disorders , 2000 .