A Case Report on Hirayama Disease

Authors

  • B. B. Sharma Department of Radio-diagnosis, SGT Medical College & Research Institute, Gurugram (Haryana), India.
  • Shashi Sharma Department of Pediatrics, SGT Medical College & Research Institute, Gurugram (Haryana), India.
  • Monu Sarin Department of Radio-diagnosis, SGT Medical College & Research Institute, Gurugram (Haryana), India.
  • Abhivind Bhutani Department of Radio-diagnosis, SGT Medical College & Research Institute, Gurugram (Haryana), India.
  • Surabhi Lathwal Department of Radio-diagnosis, SGT Medical College & Research Institute, Gurugram (Haryana), India.

DOI:

https://doi.org/10.9734/bpi/nfmmr/v9/12122D

Keywords:

Hirayama disease, spinal muscular atrophy, cervical myelopathy, MR Imaging. A

Abstract

Hirayama Disease is a non-progressive juvenile spinal muscular atrophy of the distal upper limb, Cervical myelopathy affects the dorsal aspect of the cervical cord as a result of the flexion action. It's a benign motor neuron condition with a gradual course that eventually remains stagnant. Magnetic resonance imaging in flexion is quite sensitive to these results, which may be missed in neutral position. Hirayama disease characteristically affects adolescents and young adults and presents as weakness and atrophy of the distal part of the upper limbs. We discuss a case of an adolescent boy who came with asymmetrical weakness in both hands, and whose magnetic resonance (MR) imaging in flexion indicated Hirayama disease-like alterations.

Published

2021-08-24

How to Cite

B. B. Sharma, Shashi Sharma, Monu Sarin, Abhivind Bhutani, & Surabhi Lathwal. (2021). A Case Report on Hirayama Disease . New Frontiers in Medicine and Medical Research Vol. 9, 116–123. https://doi.org/10.9734/bpi/nfmmr/v9/12122D