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<!doctype html> <html lang="ja"> <head> <title>Charcot-Marie-Hereditary Neuropathy: A Dental Disorder | 1099715</title> <meta name="keywords" content="Mariana Ribeiro, Constanca Hipolito-Reis, Claudio Ferreira, Rita Amorim Pinto Correia, "/> <meta name="description" content="Charcot-Marie-Tooth disease (CMT) is a hereditary neuropathy affecting the peripheral nervous system due to genetic mutations impacting the myelin sheath o..1099715"/> <meta name="citation_publisher" content="ロングダム出版SL" /> <meta name="citation_journal_title" content="がん研究と免疫腫瘍学ジャーナル"> <meta name="citation_title" content="Charcot-Marie-Hereditary Neuropathy: A Dental Disorder"> <meta name="citation_author" content="Mariana Ribeiro" /> <meta name="citation_author" content="Constanca Hipolito-Reis" /> <meta name="citation_author" content="Claudio Ferreira" /> <meta name="citation_author" content="Rita Amorim Pinto Correia" /> <meta name="citation_year" content=""> <meta name="citation_volume" content="0"> <meta name="citation_issue" content="0"> <meta name="citation_abstract" content="Charcot-Marie-Tooth disease (CMT) is a hereditary neuropathy affecting the peripheral nervous system due to genetic mutations impacting the myelin sheath or axon. The main types include CMT 1 (demyelinating), CMT 2 (axonal), and CMTX (X-linked CMT). Symptoms progress insidiously, starting with foot deformities and weakness in the lower limbs, potentially advancing to the upper limbs. Diagnosis involves clinical evaluation, electro diagnostic tests and genetic testing. Treatment aims to manage symptoms. This case discusses a 66-year-old man with flaccid tetra paresis and glove-and-stocking hypoesthesia, with a family history of CMT. Electromyography indicated predominantly axonal sensorimotor polyneuropathy, leading to a diagnosis of CMT 2. He is being treated in primary care with physiotherapy focused on functionality and gait. The late diagnosis stemmed from the patient underestimating his symptoms. CMT is challenging to diagnose in primary care, highlighting the need for collaboration with neurology and thorough assessments to manage the condition effectively."> <meta name="citation_abstract_html_url" content="https://japanese.longdom.org/abstract/charcotmariehereditary-neuropathy-a-dental-disorder-1099715.html"> <meta name="format-detection" content="telephone=no"> <meta http-equiv="Content-Language" content="ja"> <meta name="google-site-verification" content="NomPTP94YozsgvD3NEFpNqUfY88e0TU0L64zNzZTpd0" /> <meta itemprop="name" content="longdom" /> <meta http-equiv="X-UA-Compatible" content="IE=edge"> <meta name="ROBOTS" content="INDEX,FOLLOW"> <meta name="googlebot" content="INDEX,FOLLOW"> <meta name="viewport" content="width=device-width, initial-scale=1, shrink-to-fit=no"> <link rel="canonical" href="https://japanese.longdom.org/abstract/charcotmariehereditary-neuropathy-a-dental-disorder-1099715.html"> <link rel="alternate" 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sheath or axon. The main types include CMT 1 (demyelinating), CMT 2 (axonal), and CMTX (X-linked CMT). Symptoms progress insidiously, starting with foot deformities and weakness in the lower limbs, potentially advancing to the upper limbs. Diagnosis involves clinical evaluation, electro diagnostic tests and genetic testing. Treatment aims to manage symptoms. This case discusses a 66-year-old man with flaccid tetra paresis and glove-and-stocking hypoesthesia, with a family history of CMT. Electromyography indicated predominantly axonal sensorimotor polyneuropathy, leading to a diagnosis of CMT 2. He is being treated in primary care with physiotherapy focused on functionality and gait. The late diagnosis stemmed from the patient underestimating his symptoms. CMT is challenging to diagnose in primary care, highlighting the need for collaboration with neurology and thorough assessments to manage the condition effectively.</p> <div class="alert alert-info text-left"><b>免責事項:</b> この要約は人工知能ツールを使用して翻訳されたものであり、まだレビューまたは検証されていません。</div> <div class="nav social-icons"> <a class="nav-link w-auto">この記事をシェアする</a> <a title="ここをクリック" target="_blank" href="https://www.facebook.com/sharer.php?u=https://japanese.longdom.org/abstract/charcotmariehereditary-neuropathy-a-dental-disorder-1099715.html" rel="noopener"><i class="fab fa-facebook-f"></i></a> <a class="nav-link" title="ここをクリック" target="_blank" href="https://twitter.com/share?url=https://japanese.longdom.org/abstract/charcotmariehereditary-neuropathy-a-dental-disorder-1099715.html" rel="noopener"><i class="fab fa-twitter"></i></a> <a class="nav-link" title="ここをクリック" target="_blank" href="https://www.linkedin.com/shareArticle?mini=true&url=https://japanese.longdom.org/abstract/charcotmariehereditary-neuropathy-a-dental-disorder-1099715.html" rel="noopener"><i class="fab fa-linkedin-in"></i></a> <a class="nav-link" title="ここをクリック" target="_blank" href="https://plus.google.com/share?url=https://japanese.longdom.org/abstract/charcotmariehereditary-neuropathy-a-dental-disorder-1099715.html" rel="noopener"><i class="fab fa-google-plus-g"></i></a> </div> </div> </div> </div> </section> <footer class="bg-blue-grey-900 py-3"> <div class="container"> <div class="row"> <div class="col-12 col-sm-4"> <h4 class="white font-size-4 fweight-400 border-bottom-1 pb-2">コンテンツリンク</h4> <ul class="list-unstyled footer-links font-size-3"> <li><a class="" href="https://japanese.longdom.org/privacy-policy.html" title="ここをクリック">プライバシーポリシー</a></li> <li><a class="" href="https://japanese.longdom.org/terms-conditions.html" title="ここをクリック">利用規約</a></li> <li><a class="" href="https://japanese.longdom.org/authors-reviewers-editors.html" title="ここをクリック">著者、査読者、編集者</a></li> </ul> </div> <div class="col-12 col-sm-4"> <h4 class="white font-size-4 fweight-400 border-bottom-1 pb-2">ロングダムに連絡する</h4> <p><strong>ロングダムグループ SA</strong><br /> ロジェ・ヴァンデンドリッシュ通り、<br /> 18、1150 ブリュッセル、ベルギー<br /> 電話番号: +442038085340<br /> <strong>メール:</strong> <a class="white" href="mailto:info@longdom.org" title="ここをクリック">info@longdom.org</a></p> </div> <div class="col-12 col-sm-4"> <h4 class="white font-size-4 fweight-400 border-bottom-1 pb-2">接続</h4> <nav class="nav nav-pills social-icons-footer flex-column a-pl-0"> <a href="https://www.facebook.com/longdompublisher" title="ここをクリック" target="_blank" class="nav-link bg-facebook-hover"><i class="fab fa-facebook-f bg-facebook"></i></a> <a href="https://www.linkedin.com/company/longdom-publishing-sl/" title="ここをクリック" target="_blank" class="nav-link bg-linkedin-hover"><i class="fab fa-linkedin-in bg-linkedin"></i></a> <a href="https://twitter.com/LongdomP" title="ここをクリック" target="_blank" class="nav-link bg-twitter-hover"><i class="fab fa-twitter bg-twitter"></i></a> <a href="https://www.instagram.com/longdom_publisher/" title="ここをクリック" target="_blank" class="nav-link bg-instagram-hover"><i class="fab fa-instagram bg-instagram"></i></a> </nav> </div> </div> <div class="row text-center"> <div class="col"> <p>著作権 © 2024 <a href="https://japanese.longdom.org/" title="ここをクリック" class="white">ロングダム出版SL</a>.</p> </div> </div> </div> </footer>  <a href="#0" class="cd-top js-cd-top">Top</a>   <script src="https://code.jquery.com/jquery-3.3.1.min.js"></script> <script src="https://cdnjs.cloudflare.com/ajax/libs/popper.js/1.14.7/umd/popper.min.js"></script> <script src="https://stackpath.bootstrapcdn.com/bootstrap/4.3.1/js/bootstrap.min.js"></script>  <script> jQuery(function($) { $(window).scroll(function fix_element() { $('#target').css( $(window).scrollTop() > 100 ? 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