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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338714 | PMC |
| http://dx.doi.org/10.11604/pamj.2022.42.48.29515 | DOI Listing |
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Postural Tremor Caused by Hirayama Disease Mimicking Essential Tremor.
Tremor Other Hyperkinet Mov (N Y)
December 2024
National Clinical Research Center for Geriatric Disorders, Changsha, Hunan 410078, China.
Background: Postural tremor is a common clinical situation. Timely and accurate diagnosis is essential for effective treatment. However, clinicians often encounter difficulties distinguishing between essential tremor and other etiologies due to overlapping symptoms and atypical features.
View Article and Find Full Text PDFFive Years of Follow-up after Posterior Cervical Fusion Surgery for Hirayama Disease:A Case Report.
J Med Invest
October 2024
Department of Orthopedics, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, Japan.
Background: Hirayama disease (HD) is characterized by slow progression of muscle atrophy without sensory disturbance in a single upper extremity in adolescent boys. HD can be treated using both conservative measures and surgery. However, the optimal treatment remains controversial.
View Article and Find Full Text PDFA Case Report and Review of Literature on Hirayama Disease.
Cureus
August 2024
Neurological Surgery, Nizam's Institute of Medical Sciences, Hyderabad, IND.
Hirayama disease (HD) is a rare, benign, self-limiting condition that typically affects individuals in their 20s. Although the disease is self-limiting, it can result in functional impairment in those affected. The most common presentation is an asymmetrical, unilateral, or bilateral upper limb weakness with wasting.
View Article and Find Full Text PDFHirayama Disease: Surgical Restoration of Hand Function.
J Hand Surg Am
August 2024
Division of Hand Surgery, Department of Orthopedic Surgery, Mayo Clinic, Rochester, MN, USA. Electronic address:
Purpose: Hirayama disease (HD) is a rare, nonfamilial, self-limiting, progressive lower cervical myelopathy, resulting in debilitating distal upper-extremity motor deficits, mimicking high ulnar neuropathy, lower trunk brachial plexopathy, or C8-T1 radiculopathy. Although most literature focuses on pathophysiology and prevention of disease progression, there remains limited discussion regarding treatment to improve upper-extremity function in patients with stable disease. The upper-extremity manifestations of HD are reviewed along with surgical options for restoring hand function.
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