Hirayama Disease (monomelic amyotrophy)

Hirayama disease (HD) or monomelic amyotrophy (MA) is a rare muscular atrophy that affects young Asian males, usually occurs in one of the upper limbs that progresses slowly. It is diagnosed by means of electromyographic/electroneurographic conduction speed studies and by magnetic resonance imaging (MRI) of the spinal cord. In this paper two different HD case is reported

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1. Jin X, Jiang JY, Lu FZ, Xia XL, Wang LX, Zheng CJ. Electrophysiological differences between Hirayama disease, amyotrophic lateral sclerosis and cervical spondylotic amyotrophy. BMC Musculoskelet Disord. 2014;15:349.

2. Anuradha S, Fanai V. Hirayama Disease: A Rare Disease with Unusual Features. Case Rep Neurol Med. 2016;2016:5839761.

3. Yoldaş TK, Çoruh Y, Keklikoglu HD, Polat HG, Güven B. Hirayama Hastalığı. Fırat Tıp Dergisi 2008;13(4):274-6.

4. Yuksel M, Kalemci O, Yuksel KZ, Erguden C, Yucesoy K. Hirayama hastalığı ve tanıda Manyetik Rezonans görüntülemenin önemi. Sinir Sistemi Cerrahisi Derg. 2009;2(4):191-5.

5. Ozturker C. Kara K, Incedayi M, Sonmez G, Mutlu H.. Hirayama disease. Spine J. 2016;16(5):299-300.

6. Patel DR, Knepper L, Jones HR Jr. Late-onset monomelic amyotrophy in a Caucasian woman. Muscle Nerve. 2008;37(1):115-9.

7. Basil T. Darras, Jennifer A. Markowitz, Umrao R. Monani, Darryl C. De Vivo. Spinal Muscular Atrophies In: Neuromuscular Disorders of Infancy, Childhood, and Adolescence: A Clinician's Approach. 2nd edition, Elsevier, London, 2014: 117-45.
Medicine Science-Cover
  • ISSN: 2147-0634
  • Yayın Aralığı: Yılda 4 Sayı
  • Başlangıç: 2012
  • Yayıncı: Effect Publishing Agency ( EPA )
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