Monomelic amyotrophy
| Monomelic amyotrophy | |
|---|---|
| Classification and external resources | |
| ICD-10 | G71.8 |
| OMIM | 602440 |
| MeSH | C538253 |
| Orphanet | 65684 |
Monomelic amyotrophy (MMA), also known as Hirayama disease and Spinal muscular atrophy juvenile nonprogressive — is an untreatable, focal motor neuron disease that primarily affects young (15- to 25-year-old) males in India and Japan. MMA is marked by insidious onset of muscular atrophy, which stabilizes at a plateau after two to five years from which it neither improves nor worsens.[1][2][3] There is no pain or sensory loss associated with MMA. Unlike other lower motor neuron diseases, MMA is not believed to be hereditary and fasciculations (involuntary muscle twitches) are rare.EMG tests reveal loss of the nerve supply, or denervation, in the affected limb without conduction block (nerve blockage restricted to a small segment of the nerve). Increased sweating, coldness and cyanosis have been reported for a few patients, indicating involvement of the sympathetic nervous system.While MMA will cause weakness and/or wasting in only one limb, EMG and NCV tests often show signs of reinnervation in the unaffected limbs.
Symptoms
Patient feels contracture of middle and ring finger. Slight thinning of the subdigital Palm of the affected fingers. Initial pain and weakness subside with preliminary treatment with antiinflammatories, and B-complex vitamins. Initial loss of function improves almost fully.
Treatment
There is no cure for MMA. Treatment consists of muscle strengthening exercises and training in hand coordination. It has been proposed that the changes in this disease are from compression of the spinal cord in flexion due to forward shifting of the posterior dural sac.[4] There have been treatments studies ranging from use of a cervical collar[5] to anterior cervical fusion and posterior decompression.[6]
Prognosis
The symptoms of MMA usually progress slowly for one to two years before reaching a plateau, and then remain stable for many years. Disability is generally slight. Rarely, the weakness progresses to the opposite limb. There is also a slowly progressive variant of MMA known as O'Sullivan-McLeod syndrome, which only affects the small muscles of the hand and forearm and has a slowly progressive course.
Epidemiology
MMA mostly occurs in males between the ages of 15 and 25. Onset and progression are slow. MMA is seen most frequently in Asia, particularly in Japan and India; it is much less common in North America.
References
- ↑ "Monomelic Amyotrophy Information Page | National Institute of Neurological Disorders and Stroke". www.ninds.nih.gov. Retrieved 23 December 2016.
- ↑ "Monomelic amyotrophy | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Retrieved 23 December 2016.
- ↑ Liewluck, Teerin; Saperstein, David S (November 2015). "Progressive Muscular Atrophy". In Dimachkie, Mazen M.; Barohn, Richard J. Motor Neuron Disease, An Issue of Neurologic Clinics. Elsevier Health Sciences. p. 766. ISBN 9780323413459.
- ↑ Lai V, Wong YC, Poon WL, Yuen MK, Fu YP, Wong OW (December 2011). "Forward shifting of posterior dural sac during flexion cervical magnetic resonance imaging in Hirayama disease: an initial study on normal subjects compared to patients with Hirayama disease". Eur J Radiol (primary source). 80 (3): 724–8. PMID 20727701. doi:10.1016/j.ejrad.2010.07.021.
- ↑ Hassan KM, Sahni H (2013). "Nosology of juvenile muscular atrophy of distal upper extremity: from monomelic amyotrophy to Hirayama disease--Indian perspective". Biomed Res Int. 2013: 478516. PMC 3770029
. PMID 24063005. doi:10.1155/2013/478516. - ↑ Lin MS, Kung WM, Chiu WT, Lyu RK, Chen CJ, Chen TY (June 2010). "Hirayama disease". J Neurosurg Spine. 12 (6): 629–34. PMID 20515348. doi:10.3171/2009.12.SPINE09431.
Further reading
- Di Muzio, A.; Pizzi, C. D.; Lugaresi, A.; Ragno, M.; Uncini, A. (1994). "Benign monomelic amyotrophy of lower limb: A rare entity with a characteristic muscular CT". Journal of the Neurological Sciences. 126 (2): 153–161. PMID 7853021. doi:10.1016/0022-510X(94)90266-6.
- Di Guglielmo, G.; Brahe, C.; Di Muzio, A.; Uncini, A. (1996). "Benign monomelic amyotrophies of upper and lower limb are not associated to deletions of survival motor neuron gene". Journal of the Neurological Sciences. 141 (1–2): 111–113. PMID 8880702. doi:10.1016/0022-510X(96)00154-2.
- Münchau, A.; Rosenkranz, T. (2000). "Benign Monomelic Amyotrophy of the Lower Limb – Case Report and Brief Review of the Literature". European Neurology. 43 (4): 238–240. PMID 10828656. doi:10.1159/000008183.
- Freitas, M. R. G. D.; Nascimento, O. J. M. (2000). "Benign monomelic amyotrophy: A study of twenty-one cases" (PDF). Arquivos de Neuro-Psiquiatria. 58 (3B): 808–813. PMID 11018815. doi:10.1590/S0004-282X2000000500003.
- Gourie-Devi, M.; Nalini, A. (2001). "Sympathetic skin response in monomelic amyotrophy". Acta Neurologica Scandinavica. 104 (3): 162–166. PMID 11551236. doi:10.1034/j.1600-0404.2001.00016.x.
- Neves, M. A. O.; Freitas, M. R. G. D.; Mello, M. P. D.; Dumard, C. H.; Freitas, G. R. D.; Nascimento, O. J. M. (2007). "Benign monomelic amyotrophy with proximal upper limb involvement: Case report". Arquivos de Neuro-Psiquiatria. 65 (2b): 524–527. PMID 17665029. doi:10.1590/S0004-282X2007000300032.
