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Hirayama Hastalığı (Monomelik Amyotrofi)

Year 2008, Volume: 13 Issue: 4, 274 - 276, 01.08.2008
https://izlik.org/JA57HB42NE

Abstract

Hirayama Hastalığı (HH), genç erkeklerde daha sık görülen benign bir alt motor nöron hastalığıdır. Distal ekstremiteyi tutan ilerleyici güçsüzlük ve sinsi başlangıç ile karekterizedir. Genellikle başlangıcından sonra 5 yıl içinde stabilize olan, benign ve nonprogresif bir hastalık olarak kabul edilir. Biz bu bildiride duysal yakınmanın eşlik etmediği progresif amyotrofi bulguları olan 23 yaşında bir kadın hastayı sunuyoruz.©2008, Fırat Üniversitesi, Tıp Fakültesi

References

  • Fetoni V, Briem E, Carrara F, Mora M, Zeviani M. Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNA gene. Neuromusculer Disorders 2004; 14: 723-726.
  • Tunçbay T, Tunçbay E. Nöromüsküler Hastalıklar. İzmir: Ege Üniversitesi Basım Evi, 2000: 136-140. 3. Hirayama K,Toyokura Y, Tsubaki T. Juvenile musculer atrophy unilateral upper extremity- a new clinical entity. Psychiatr Neurol Jpn 1959; 61: 2190-2197.
  • Gourie Devi M, Nalini A. Long term follow-up of 44 patients with brachial monomelic amyotrophy. Acta Neurol Scand 2003; 107: 215-220.
  • Nalini A, Lokesh E, Ratnavalli E. Familial monomelic amyotrophy: a case report from India. Journal of Neurological Sciences 2004; 220: 95-98.
  • Massa R, Scalise A, Iani C, Palmieri MG, Bernardi G. Delayed focal involvement of upper motor neurons in the Madras pattern of motor neuron disease. Electroencephalography and clinical Neurophysiology 1998; 109: 523-526.
  • Hamano T, Mutoh T, Hirayama M, Ito K, Kimura M, and et al. MRI findings of bening monomelic amyotrophy of lower limb. J neurological Sciences 1999; 165: 184-187.
  • Münchau A, Rosenkranz T. Benign Monomelic Amyotrophy of the lower limb- case report and brief review of the Literature. Eur Neurol 2000; 43: 238-240.
  • Gourei Devi M, Nalini A. Sympathetic skin response in monomelic amyotrophy. Acta Neurol Scand 2001; 104: 162-166.
  • Rowin J, Meriggioli MN, Cochran EJ. Monomelic amyotrophy with late progression. Neuromusculer Disorder 2001; 11: 305- 308.
  • Sullivan O, McLeod J. Distal chronic spinal muscular atrophy involving the hands. J Neurol Neurosurg Psychiatry 1978; 41: 653-658.
  • Kiernan MC, Lethlean AK, Blum PW. Monomelic amyotrophy: non progressive atrophy of the upper limb. J.Clinical Neuroscience.1999; 6: 353-355
  • Schroder R, Keller E, Flacke S, Schmidt S, Pohl C, Klockgether T,et al. MRI findings in Hirayama’s Disease: flexion- inducedcervical myelopathy or intrinsic motor neuron disease? J Neurol 1999; 246: 1069-1074.
  • Kabul Tarihi:22.11.2007

Hirayama Disease (Monomelic Amyotrophy)

Year 2008, Volume: 13 Issue: 4, 274 - 276, 01.08.2008
https://izlik.org/JA57HB42NE

Abstract

Hirayama Disease (HD) is a benign lower motor neuron disorder in the young with male preponderance. It is characterized by insidious onset and progressive weakness and wasting of a distal extremity . Generally, this disease is considered a 'benign' and non-progressive motor neuron disease, which stabilizes within five years of onset.We describe a 23-year-old famele patient who experienced progressive amyotrophy with no sensorial abnormality.©2008, Firat University, Medical Faculty.

References

  • Fetoni V, Briem E, Carrara F, Mora M, Zeviani M. Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNA gene. Neuromusculer Disorders 2004; 14: 723-726.
  • Tunçbay T, Tunçbay E. Nöromüsküler Hastalıklar. İzmir: Ege Üniversitesi Basım Evi, 2000: 136-140. 3. Hirayama K,Toyokura Y, Tsubaki T. Juvenile musculer atrophy unilateral upper extremity- a new clinical entity. Psychiatr Neurol Jpn 1959; 61: 2190-2197.
  • Gourie Devi M, Nalini A. Long term follow-up of 44 patients with brachial monomelic amyotrophy. Acta Neurol Scand 2003; 107: 215-220.
  • Nalini A, Lokesh E, Ratnavalli E. Familial monomelic amyotrophy: a case report from India. Journal of Neurological Sciences 2004; 220: 95-98.
  • Massa R, Scalise A, Iani C, Palmieri MG, Bernardi G. Delayed focal involvement of upper motor neurons in the Madras pattern of motor neuron disease. Electroencephalography and clinical Neurophysiology 1998; 109: 523-526.
  • Hamano T, Mutoh T, Hirayama M, Ito K, Kimura M, and et al. MRI findings of bening monomelic amyotrophy of lower limb. J neurological Sciences 1999; 165: 184-187.
  • Münchau A, Rosenkranz T. Benign Monomelic Amyotrophy of the lower limb- case report and brief review of the Literature. Eur Neurol 2000; 43: 238-240.
  • Gourei Devi M, Nalini A. Sympathetic skin response in monomelic amyotrophy. Acta Neurol Scand 2001; 104: 162-166.
  • Rowin J, Meriggioli MN, Cochran EJ. Monomelic amyotrophy with late progression. Neuromusculer Disorder 2001; 11: 305- 308.
  • Sullivan O, McLeod J. Distal chronic spinal muscular atrophy involving the hands. J Neurol Neurosurg Psychiatry 1978; 41: 653-658.
  • Kiernan MC, Lethlean AK, Blum PW. Monomelic amyotrophy: non progressive atrophy of the upper limb. J.Clinical Neuroscience.1999; 6: 353-355
  • Schroder R, Keller E, Flacke S, Schmidt S, Pohl C, Klockgether T,et al. MRI findings in Hirayama’s Disease: flexion- inducedcervical myelopathy or intrinsic motor neuron disease? J Neurol 1999; 246: 1069-1074.
  • Kabul Tarihi:22.11.2007
There are 13 citations in total.

Details

Primary Language Turkish
Authors

Tahir Kurtuluş Yoldaş This is me

Yıldız Çoruh This is me

Hava Dönmez Keklikoğlua This is me

Hayriye Gül Polat This is me

Bülent Güven This is me

Publication Date August 1, 2008
IZ https://izlik.org/JA57HB42NE
Published in Issue Year 2008 Volume: 13 Issue: 4

Cite

APA Yoldaş, T. K., Çoruh, Y., Keklikoğlua, H. D., Polat, H. G., & Güven, B. (2008). Hirayama Hastalığı (Monomelik Amyotrofi). Fırat Tıp Dergisi, 13(4), 274-276. https://izlik.org/JA57HB42NE
AMA 1.Yoldaş TK, Çoruh Y, Keklikoğlua HD, Polat HG, Güven B. Hirayama Hastalığı (Monomelik Amyotrofi). Fırat Tıp Dergisi. 2008;13(4):274-276. https://izlik.org/JA57HB42NE
Chicago Yoldaş, Tahir Kurtuluş, Yıldız Çoruh, Hava Dönmez Keklikoğlua, Hayriye Gül Polat, and Bülent Güven. 2008. “Hirayama Hastalığı (Monomelik Amyotrofi)”. Fırat Tıp Dergisi 13 (4): 274-76. https://izlik.org/JA57HB42NE.
EndNote Yoldaş TK, Çoruh Y, Keklikoğlua HD, Polat HG, Güven B (August 1, 2008) Hirayama Hastalığı (Monomelik Amyotrofi). Fırat Tıp Dergisi 13 4 274–276.
IEEE [1]T. K. Yoldaş, Y. Çoruh, H. D. Keklikoğlua, H. G. Polat, and B. Güven, “Hirayama Hastalığı (Monomelik Amyotrofi)”, Fırat Tıp Dergisi, vol. 13, no. 4, pp. 274–276, Aug. 2008, [Online]. Available: https://izlik.org/JA57HB42NE
ISNAD Yoldaş, Tahir Kurtuluş - Çoruh, Yıldız - Keklikoğlua, Hava Dönmez - Polat, Hayriye Gül - Güven, Bülent. “Hirayama Hastalığı (Monomelik Amyotrofi)”. Fırat Tıp Dergisi 13/4 (August 1, 2008): 274-276. https://izlik.org/JA57HB42NE.
JAMA 1.Yoldaş TK, Çoruh Y, Keklikoğlua HD, Polat HG, Güven B. Hirayama Hastalığı (Monomelik Amyotrofi). Fırat Tıp Dergisi. 2008;13:274–276.
MLA Yoldaş, Tahir Kurtuluş, et al. “Hirayama Hastalığı (Monomelik Amyotrofi)”. Fırat Tıp Dergisi, vol. 13, no. 4, Aug. 2008, pp. 274-6, https://izlik.org/JA57HB42NE.
Vancouver 1.Yoldaş TK, Çoruh Y, Keklikoğlua HD, Polat HG, Güven B. Hirayama Hastalığı (Monomelik Amyotrofi). Fırat Tıp Dergisi [Internet]. 2008 Aug. 1;13(4):274-6. Available from: https://izlik.org/JA57HB42NE