Charcot-Marie-Tooth (CMT) disease, which encompasses several hereditary motor and sensory neuropathies, is one of the most common neuro-muscular disorders. 80% of patients having CMT disease are diagnosed with per cavus deformity. Orthosis is widespread and varies widely in forms. The paper arises the necessity of habilitation at the earliest possible stage as only a few patients use it. The meta-analysis of 412 scientific papers concerning this problem demonstrates the getting better gate, balance and the stopping CMT progression which is scientifically proven. It is also shown that patients with CMT use low prevalence of orthotics, and demonstrate low compliance of patients (for various reasons), high expectations from this habilitation technique.
References
[1]
El-Abassi, R., England, J.D. and Carter, G.T. (2014) Charcot-Marie-Tooth Disease: An Overview of Genotypes, Phenotypes, and Clinical Management Strategies. PM & R, 4, 342-355. https://doi.org/10.1016/j.pmrj.2013.08.611
[2]
Johnson, N.E., Heatwole, C.R., Dilek, N., Sowden, J., Kirk, C.A., Shereff, D., Shy, M.E. and Herrmann, D.N. (2014) On Behalf of the Inherited Neuropathies Consortium. Quality-of-Life in Charcot Marie Tooth Disease: The Patient’s Perspective. Neuromuscular Disorder, 11, 1018-1023. https://doi.org/10.1016/j.nmd.2014.06.433
[3]
Piazza, S., Ricci, G., CaldarazzoIenco, E., Carlesi, C., Volpi, L., Siciliano, G. and Mancuso, M. (2010) Pes Cavus and Hereditary Neuropathies: When a Relationship Should Be Suspected. Journal of Orthopaedics and Traumatology, 11, 195-201. https://doi.org/10.1007/s10195-010-0114-y
[4]
Houlden, H., Charlton, P. and Singh, D. (2007) Neurology and Orthopaedic. Journal of Neuralology, Neurosurgery, and Psychiatry, 78, 224-232. https://doi.org/10.1136/jnnp.2006.092072
[5]
Joo, S.Y., Choi, B.-O., Kim, D.Y., Jung, S.J., Cho, S.Y. and Hwang, S.J. (2011) Foot Deformity in Charcot Marie Tooth Disease according to Disease Severity. Annals of Rehabilitation Medicine, 4, 499-506.
[6]
Maranho, D.A. and Volpon, J.B. (2009) Acquired Res Cavus in Charcoy-Marie-Tooth Disease. Revista Brasileira de Orthopedia, 6, 479-486. https://doi.org/10.1590/S0102-36162009000600004
[7]
Hoellwarth, J.S., Mahan, S.T. and Spencer, S.A. (2012) Painful Pes Planovalgus: An Uncommon Pediatric Orthopedic Presentation of Charcot-Marie-Tooth Disease. Journal of Pediatric Orthopaedic B, 5, 428-433. https://doi.org/10.1097/BPB.0b013e3283563750
[8]
Alexander, I.J. and Johnson, K.A. (1989) Assessment and Management of Per Cavus in Charcout-Marie-Tooth Disease. Clinical Orthopaedics and Related Research, 246, 273-281.
[9]
Nagai, M.K., Chan, G., Guille, J.T., Kumar, S.J., Scavina, M. and Mackenzie, W.G. (2006) Prevalence of Charcout-Marie-Tooth Disease in Patients Who Have Bilateral Cavovarus Feet. Journal of Pediatric Orthopaedics, 4, 438-443. https://doi.org/10.1097/01.bpo.0000226278.16449.c4
[10]
Wicart, P. (2012) Cavus Foot, From Neonates to Adolescents. Orthopaedics and Traumatology: Surgery and Research, 98, 813-828. https://doi.org/10.1016/j.otsr.2012.09.003
[11]
Laurá, M., Singh, D., Ramdharry, G., Morrow, J., Skorupinska, M., Pareyson, D., Burns, J., Lewis, R.A., Scherer, S.S., Herrmann, D.N., Cullen, N., Bradish, C., Gaiani, L., Martinelli, N., Gibbons, P., Pfeffer, G., Phisitkul, P., Wapner, K., Sanders, J., Flemister, S., Shy, M.E., Reilly, M.M., Inherited Neuropathies Consortium. (2018) Prevalence and Orthopedic Management of Foot and Ankle Deformities in Charcot-Marie-Tooth Disease. Muscle Nerve, 57, 255-259. https://doi.org/10.1002/mus.25724
[12]
McCorquodale, D., Pucillo, E.M. and Johnson, N.E. (2016) Management of Charcout-Marie-Tooth Disease: Improving Long-Term Care with a Multidisciplinary Approach. Journal of Multidisciplinary Healthcare, 9, 7-11.
[13]
Skalsky, A.J. and McDonald, C.M. (2012) Prevention and Management of Limb Contractures in Neuromuscular Disease. Physical Medicine & Rehabilitation Clinics of North America, 3, 675-687. https://doi.org/10.1016/j.pmr.2012.06.009
[14]
Birch, J.G. (1998) Orthopedic Management of Neuromuscular Disorders in Children. Seminars in Pediatric Neurology, 5, 78-91. https://doi.org/10.1016/S1071-9091(98)80024-7
[15]
Guillebaste, B., Calmels, P. and Rougier, P.R. (2011) Assessment of Appropriate Ankle-Foot Orthoses Models for Patient with Charcout-Marie-Tooth Disease. American Journal of Physical Medicine & Rehabilitation, 90, 619-627. https://doi.org/10.1097/PHM.0b013e31821f7172
[16]
Rose, K.J., Raymond, J., Refshauge, K., North, K.N. and Burns, J. (2010) Serial Nights Casting Increases Ankle Dorsiflexion Range in Children and Young Adults with Charcout-Marie-Tooth Disease: A Randomized Trial. Journal of Psysiotherapy, 56, 113-119. https://doi.org/10.1016/S1836-9553(10)70041-2
[17]
Ramdharry, G.M., Day, B.L., Reilly, M.M. and Marsden, J.F. (2012) Foot Drop Splints Improve Proximal as Well as Distal Leg Control during Gait in Charcout-Marie-Tooth Disease. Muscle Nerve, 46, 512-519. https://doi.org/10.1002/mus.23348
[18]
Kozhevnikov, O.V., Kosov, I.S., Ivanov, A.V., Gribova, I.V. and Bo-lotov, A.V. (2015) Comparative Evaluation of the Results of Complex and Conservative Treatment of Flat-Calf Deformities of the Feet in Children. Bulletin of Traumatology and Orthopedics, 2, 55-59.
[19]
Mnatsakanian, A., Kissel, J.T., Terry, P. and King, W.M. (2017) One Clinic’s Experience with Carbon Fiber Orthoses in Neuromuscular Disease. Muscle and Nerve, 2, 202-205. https://doi.org/10.1002/mus.25233
[20]
Uygur, F., Bek, N., Kuklu, B. and Yilmaz, O. (2001) Orthotic Management of the Lower Limb in Children with Hereditary Motor Sensory Neuropathy (NMSN). Prosthetics and Orthotics International, 25, 139-143. https://doi.org/10.1080/03093640108726587
[21]
Anens, E., Emtner, M. and Hellstrom, K. (2015) Exploratory Study of Physical Activity in Persons with Charcot-Marie-Tooth Disease. Archives of Physical Medicine and Rehabilitation, 2, 260-268. https://doi.org/10.1016/j.apmr.2014.09.013
[22]
Phillips, M.F., Robertson, Z., Killen, B. and White, B. (2012) A Pilot Study of a Rossover Trial with Randomized Use of Ankle-Foot Orthoses for People with Charcot-Marie-Tooth Disease. Clinical Rehabilitation, 9, 534-544. https://doi.org/10.1177/0269215511426802
[23]
Rose, K.J., Hiller, C.E., Mandarakas, M., Raymond, J., Refshauge, K. and Burns, J. (2015) Correlates of Functional Ankle Instability in Children and Adolescents with Charcot-Marie-Tooth Disease. Journal of Foot and Ankle Research, 8, 61. https://doi.org/10.1186/s13047-015-0118-1
[24]
Wegener, C., Wegener, K., Smith, R., Schott, K.H. and Burns, J. (2015) Biomechanical Effects of Sensorimotor Orthoses in Adults with Charcot-Marie-Tooth Disease. Journal of Foot and Ankle Re-search, 2, 39. https://doi.org/10.1186/1757-1146-8-S2-O39
[25]
LoPiccolo, M., Chilvers, M., Graham, B. and Manoli, A. (2010) Effectiveness of the Cavus Foot Orthosis. Journal of Surgical Orthopaedic Advances, 3, 166-169.
[26]
Ortlieb, A., Olivier, J., Bouri, M., Bleuler, H. and Kuntzer, T. (2015) From Gait Measurements to Design of Assistive Orthoses for People with Neuromuscular Diseases. Proceedings of the IEEE\RAS-EMBS International Conference on Rehabilitation Robotics, Singapore, 11-14 August 2015, 368-373. https://doi.org/10.1109/ICORR.2015.7281227
[27]
Maynou, C., Szymanski, C. and Thiounn, A. (2017) The Adult Cavus Foot. EFORT Open Reviews, 2, 221-229. https://doi.org/10.1302/2058-5241.2.160077
[28]
Georgiev, H. and Georgiev, G.P. (2014) Talectomy for Equinovarus Deformity in Family Members with Hereditary Motor and Sensory Neuropathy Type I. Case Reports in Orthopedics, 2014, Article ID: 643480. https://doi.org/10.1155/2014/643480
[29]
Zhou, Y., Zhou, B., Liu, J., Tan, X., Tao, X., Chen, W. and Tang, K. (2014) A Prospective Study of Midfoot Osteotomy Combined with Adjacent Joint Sparing Internal Fixation in Treatment of Rigid Pes Cavus Deformity. Journal of Orthopaedic Surgery and Research, 9, 44. https://doi.org/10.1186/1749-799X-9-44
[30]
Hoyle, J.C., Isfort, M.C., Roggenbuck, J. and Arnold, W.D. (2015) The Genetics of Charcot-Marie-Tooth Disease: Current Trend Sand Future Implications for Diagnosis and Management. The Application of Clinical Genetics, 8, 235-243.
[31]
Chetlin, R.D., Gutmann, L. and Tarnopolsky, M. (2004) Resistance Training Effectiveness in Patients with Charcot-Marie-Tooth Disease: Recommendations for Exercise Prescription. Archives of Physical Medicine and Rehabilitation, 8, 1217-1223. https://doi.org/10.1016/j.apmr.2003.12.025
[32]
Vinci, P. and Gargiulo, P. (2008) Poor Compliance with Ankle-Foot Orthoses in Charcot-Marie-Tooth Disease. European Journal of Physical and Rehabilitation Medicine, 1, 27-31.
[33]
Shnayder, N.A., Goncharova, S.I., Duzackova, A.V., Popova, T.E., Dmitrenko, D.V., Kantimirova, E. and Shevchenko, S.A. (2015) Supposed Barriers and Motivators to Physical Activity in Patients with Charcot-Marie-Tooth Disease. Siberian Medical Review, 2, 15-25. https://doi.org/10.20333/25000136-2015-2-15-25
[34]
Shnayder, N.A., Petryaeva, O.V., Artyukhov, I.P., Sapronova, M.R. and Loginova, I.O. (2017) A Rare Case of Charcot-Mari-Tooth Disease Type 2S in a 20-Year-Old Man. International Journal of Biomedicine, 4, 324-326. https://doi.org/10.21103/Article7(4)_CR1
[35]
Kalane, U.D., Datar, C. and Mahadevan, A. (2015) First Reported Case of Charcot Marie Tooth Disease Type 4C in a Child from India with SH3TC2 Mutation But Absent Spinal Deformities. Neurology India, 3, 395-398. https://doi.org/10.4103/0028-3886.158222
[36]
The Social Network for Communicating People with CMT, Russia. https://vk.com/cmtarus
[37]
A Patient Network and Real-Time Research Plat-form, USA. https://www.patientslikeme.com/patients
[38]
CMT Support Group and Discussion Community, USA. https://www.inspire.com/groups/charcot-marie-tooth-cmt/
[39]
CMT Support Group. https://www.dailystrength.org/group/charcot-marie-tooth-disease
[40]
The Alliance of Rare Diseases, France. http://forums.maladiesraresinfo.org/maladie-charcot-marie-tooth-f200.html
[41]
The Charcot-Marie-Tooth Association, USA. https://www.cmtausa.org/index.php
[42]
Danilov, D.S. (2008) Individual Choice of Modern Pharmacotherapy of Schizophrenia (Basic Principles, Discussion of the Results of Clinical Studies and Some Practical Recommendations). Psychiatry and Pharmacotherapy, 10, 50-57.
[43]
Gluschenko, E.V., Shnayder, N.A., Kantimirova, E., Kozulina, E.A., Voevoda, M.I., Maximov, V. and Allakhverdyan, A.A. (2012) Experience in Organizing of Diagnostic and Medical and Social Care to Patients with Hereditary Neuropathy Charcot-Marie-Tooth in the Krasnoyarsk Region. Neuromuscular Disease, 1, 41-53.
[44]
Gluschenko, E.V. (2012) Case of Hereditary Motor-Sensory Neuropathy Charcot-MarieTooth of Type 1. Siberian Medical Review, 4, 84-87.
[45]
Cramer, J.A., Scheyer, R.D. and Mattson, R.H. (1990) Compliance Declines between Clinic Visits. Archives of Internal Medicine, 7, 1509-1510. https://doi.org/10.1001/archinte.1990.00390190143023
[46]
Naumova, E.A. and Schvartc, Yu.G. (2006) Performing by Patients the Medical Prescriptions: Whether Effective Are Interventions Aimed to Improve This Indicator. International Journal of Medical Practice, 1, 48-60.
[47]
Schnayder, N.A., Gluschenko, E.V. and Kozulina, E.A. (2011) Assessment of the Life Quality in Patients with Hereditary Neuropathy Charcot Marie-Tooth in the Krasnoyarsk Region. Bulletin of Siberian Medicine, 2, 57-62.
[48]
Vinci, P., Gargiulo, P., Panunzi, M. and Baldini, L. (2009) Psychological Distress in Patients with Charcot-Marie-Tooth Disease. European Journal of Physical and Rehabilitation Medicine, 3, 385-389.