Examination of cardiovascular reactivity in patients with hereditary neuropathy
Authors:
O. Horáček 1,3; D. Jílková 2; M. Matouš 2,3; R. Mazanec 4; J. Nedělka 5; P. Kolář 3; T. Nedělka 4,5
Authors‘ workplace:
Rehabilitační centrum Nemocnice Beroun, lékařský ředitel MUDr. J. Calta
1; Institut sportovního lékařství, ředitel MUDr. J. Dostal, primář MUDr. M. Matouš
2; Klinika rehabilitace a tělovýchovného lékařství 2. LF UK a FN Motol, Praha, přednosta prof. PaedDr. P. Kolář, Ph. D.
3; Neurologická klinika dospělých, FN Motol, přednosta doc. MUDr. P. Marusič, Ph. D.
4; Rehabilitace Nedělka – Poliklinika Řepy, Praha, primář MUDr. J. Nedělka
5
Published in:
Rehabil. fyz. Lék., 21, 2014, No. 3, pp. 130-135.
Category:
Original Papers
Overview
The hereditary motor and sensitive neuropathy, morbus Charcot Marie Tooth, is one of the most common neuromuscular diseases in the world. In recent years a proofs suggesting, that illness has an autonomic component were found. On a group of 17 patients suffering from Charcot Marie Tooth disease we executed a study focused on the examination of autonomic nervous system. For the most of patients, the symptoms of autonomic neuropathy were proved. Some of examined patients described subjective problems, especially gastrointestinal and sudomotor troubles. The autonomic neuropathy is also risk factor of cardiovascular morbidity, which is in relation with motor handicap and common deconditioning of patients with neuropathy important factor in deteriorating quality of life and health.
Keywords:
hereditary motor and sensitive neuropathy; morbus Charcot Marie Tooth; autonomic neuropathy; heart rate variability; spiroergometry; six minute walk test; International physical activity questionnaire; CMT Neuropathy score
Sources
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Physiotherapist, university degree Rehabilitation Sports medicineArticle was published in
Rehabilitation and Physical Medicine
2014 Issue 3
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