Literature DB >> 14964585

Advanced Hirayama disease with successful improvement of activities of daily living by operative reconstruction.

Susumu Chiba1, Kazumi Yonekura, Michio Nonaka, Tomihiro Imai, Hiroyuki Matumoto, Takuro Wada.   

Abstract

Juvenile muscular atrophy of the distal upper extremity (Hirayama disease) is a benign and non-progressive motor neuron disease. Application of a cervical collar is believed to prevent progression of symptoms in the early stages, but there is no effective therapy for the advanced disease. We found that tendon transfer improved the activities of daily living (ADL) of a patient with advanced Hirayama disease. An operative reconstruction can be valuable, even in patients with Hirayama disease who have developed impaired ADL due to extensive intrinsic hand muscle atrophy.

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Year:  2004        PMID: 14964585     DOI: 10.2169/internalmedicine.43.79

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


  14 in total

1.  Angiographically proven cervical venous engorgement: a possible concurrent cause in the pathophysiology of Hirayama's myelopathy.

Authors:  Elisa F Ciceri; Luisa Chiapparini; Alessandra Erbetta; Laura Longhi; Benedetta Cicardi; Nicoletta Milani; Carlo Lazzaro Solero; Mario Savoiardo
Journal:  Neurol Sci       Date:  2010-09-21       Impact factor: 3.307

2.  Supercharged End-to-Side Anterior Interosseous to Ulnar Motor Nerve Transfer for Hirayama Disease: A Case Report.

Authors:  Aleixo Abreu Tanure; Luis Guilherme Rosifini Alves Rezende; Ana Carolina Pazim; Marcel Leal Ribeiro
Journal:  Hand (N Y)       Date:  2021-12-28

3.  Hirayama disease is a pure spinal motor neuron disorder--a combined DTI and transcranial magnetic stimulation study.

Authors:  Kai Boelmans; Jörn Kaufmann; Sophie Schmelzer; Stefan Vielhaber; Malte Kornhuber; Alexander Münchau; Stephan Zierz; Charly Gaul
Journal:  J Neurol       Date:  2012-09-25       Impact factor: 4.849

4.  Hirayama disease: three cases assessed by F wave, somatosensory and motor evoked potentials and magnetic resonance imaging not supporting flexion myelopathy.

Authors:  Angelo Ammendola; Antonio Gallo; Teresa Iannaccone; Gioacchino Tedeschi
Journal:  Neurol Sci       Date:  2008-10-21       Impact factor: 3.307

5.  Hirayama disease: imaging profile of three cases emphasizing the role of flexion MRI.

Authors:  Radha Sarawagi; Sathya Narayanan; Prakash Manikka Lakshmanan; Sunitha Vellathussery Chakkalakkoombil
Journal:  J Clin Diagn Res       Date:  2014-08-20

6.  MRI findings in Hirayama disease.

Authors:  Monali Raval; Rima Kumari; Aldrin Anthony Dung Dung; Bhuvnesh Guglani; Nitij Gupta; Rohit Gupta
Journal:  Indian J Radiol Imaging       Date:  2010-11

Review 7.  Nosology of juvenile muscular atrophy of distal upper extremity: from monomelic amyotrophy to Hirayama disease--Indian perspective.

Authors:  Kaukab Maqbool Hassan; Hirdesh Sahni
Journal:  Biomed Res Int       Date:  2013-08-26       Impact factor: 3.411

8.  Clinical and radiological profile of Hirayama disease: A flexion myelopathy due to tight cervical dural canal amenable to collar therapy.

Authors:  K M Hassan; Hirdesh Sahni; Atul Jha
Journal:  Ann Indian Acad Neurol       Date:  2012-04       Impact factor: 1.383

9.  Imaging in Hirayama disease.

Authors:  Keshav Gupta; Shashank Sood; Jayesh Modi; Rajiv Gupta
Journal:  J Neurosci Rural Pract       Date:  2016 Jan-Mar

10.  Bimelic symmetric Hirayama disease: Spectrum of magnetic resonance imaging findings and comparative evaluation with classical monomelic amyotrophy and other motor neuron disease.

Authors:  Deb Kumar Boruah; Shantiranjan Sanyal; Arjun Prakash; Sashidhar Achar; Dhabal D Dhingani; Binod Sarma
Journal:  Iran J Neurol       Date:  2017-07-06
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