Top Abstract Purchase Related
Home
>
Node
>
Subnode

Anesthesia for Charcot-Marie-Tooth Disease: Case Report

Alzaben, K.R.; Samarah, O.Q.; Obeidat, S.S.; Halhouli, O.; Al Kharabsheh, M.

Middle East Journal of Anaesthesiology 23(5): 587-590

2016

ISSN/ISBN: 0544-0440
PMID: 27487647
Document Number: 688896
Charcot-Marie-Tooth disease comprises a group of disorders characterized by progressive muscle weakness and wasting. Reviewing the anaesthetic literature produced conflicting reports about the best anaesthetic options for patients with CMTD; as they are at increased risk of prolonged response to muscle relaxants, malignant hyperthermia and risks of regional anaesthesia. We present a case of the successful use of total intravenous anaesthesia with dexmedetomidine and propofol combined with caudal block using bupivacaine mixed with dexmedetomidine without any complications, for a 17 year old male patient with Charcot Marie-Tooth disease who underwent a lower limb orthopedic surgery.

Document emailed within 1 workday
Secure & encrypted payments

Anand, N.; Levine, D.B.; Burke, S.; Bansal, M. 1997: Neuropathic spinal arthropathy in Charcot-Marie-Tooth disease. A case report Journal of Bone and Joint Surgery. American Volume 79(8): 1235-1239
Roelofse, J.A.; Shipton, E.A. 1985: Anaesthesia for abdominal hysterectomy in Charcot-Marie-Tooth disease. A case report South African Medical Journal 67(15): 605-606
Chakravarty, A.; Ghosh, B.; Sengupta, S.; Mukhopadhyay, S. 2003: X-linked Charcot-Marie-Tooth disease with myokymia: report of a family Neurology India 51(3): 385-387
Nocentini, P.; Pace, M.; Cardona, G.; Piazzesi, W.; Bucciolini, M.G.; Ronchi, O. 1971: Extraesophageal nervous pathogenesis of achalasic megaesophagus. Clinical report of a family with Charcot-Marie-Tooth disease Rivista di Neurologia 41(6): 385-423
Ohnishi, A.; Aoki, A.; Yamamoto, T.; Tsuji, S. 2000: A case of Charcot-Marie-Tooth disease 1 B with Val 146Phe mutation of myelin protein zero showing a severe clinical phenotype Rinsho Shinkeigaku 40(3): 268-270
Cánovas, L.; Domínguez, M.; Diz, A.; Castro, M.; Barros, C.; Castro, A. 1998: General anesthesia using a laryngeal mask and anesthesia by epidural catheter in a case of Charcto-Marie-Tooth type i disease Revista Espanola de Anestesiologia y Reanimacion 45(10): 441-442
Gastaut, J.L.; Benaim, J.; Livet, M.O.; Philip, N. 2000: Charcot Marie Tooth disease: exacerbation in pregnancy Revue Neurologique (Paris) 156(10): 890-891
Rowińska-Marcińska, K. 1973: Electromyographic pattern of Charcot-Marie-Tooth disease Neurologia i Neurochirurgia Polska 7(6): 793-798
Zambelis, T. 2009: Small fiber neuropathy in Charcot-Marie-Tooth disease Acta Neurologica Belgica 109(4): 294-297
Hirota, K.; Muraoka, M.; Sugihara, K.; Amano, N.; Matsuki, A.; Oyama, T. 1988: Anesthetic experience of a patient with Charcot-Marie-Tooth disease Masui. Japanese Journal of Anesthesiology 37(2): 207-210
Alexander, I.J.; Johnson, K.A. 1989: Assessment and management of pes cavus in Charcot-Marie-tooth disease Clinical Orthopaedics and Related Research 246: 273-281
Perveen, S.; Mannan, S.; Hussain, A.; Kanwal, S. 2015: Charcot-Marie-Tooth type 1A disease from patient to laboratory Jpma. Journal of the Pakistan Medical Association 65(2): 206-212
Xiao, B.; Xie, J.; Yang, X.; Wu, Z.; Xiao, J.; Li, J. 2002: The clinical and pathologic features of Charcot-Marie-Tooth disease Zhonghua Nei Ke Za Zhi 41(11): 736-738
Goldber-Stern, H.; Navon, R.; Gadoth, N. 1995: Contribution of molecular genetics to the diagnosis of Charcot-Marie-Tooth disease Harefuah 128(11): 700-703
Geny, C.; Gaio, J.M.; Mallaret, M.; Goy, A.; Reymond, F.; Pegourie, B.; Yulis, J.; Perret, J.E. 1990: Charcot-Marie-Tooth disease disclosed by a treatment with vincristine in familial Hodgkin's disease Annales de Medecine Interne 141(8): 709-710
Lance, J.W.; Burke, D.J.; Pollard, J. 1978: Pseudomyotonia and tetany in a familial neuropathy resembling Charcot-Marie-Tooth disease Transactions of the American Neurological Association 103: 22-26
Sołtysińska, E.; Kabzińska, D.; Kochański, A. 2007: Mutations in the mitofusin 2 gene are the most common cause of Charcot-Marie-Tooth type 2 disease Neurologia i Neurochirurgia Polska 41(4): 350-354
Dupuis, M.; Brucher, J.M.; Gonsette, R. 1983: Anatomo-clinical study of a neuronal form of Charcot-Marie-Tooth disease Revue Neurologique (Paris) 139(11): 643-649
Niiyama, Y.; Kanaya, N.; Namiki, A. 2003: Anesthetic management for laparoscopic surgery in a patient with Charcot-Marie-Tooth disease Masui. Japanese Journal of Anesthesiology 52(5): 524-526
Likavcanová, E. 1972: Progressive neural amyotrophy--Charcot-Marie-Tooth disease affecting several members of a family Bratislavske Lekarske Listy 57(3): 361-365