Amyotrophic lateral sclerosis with damage to the upper motor neuron (clinical case)
- 作者: Zaytseva A.A.1,2, Medvedeva S.L.2, Gladkikh Y.V.2
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隶属关系:
- Tver State Medical University
- Regional Clinic Hospital
- 期: 卷 36, 编号 3 (2025)
- 页面: 77-80
- 栏目: From Practice
- URL: https://journals.eco-vector.com/0236-3054/article/view/678117
- DOI: https://doi.org/10.29296/25877305-2025-03-14
- ID: 678117
如何引用文章
详细
A clinical case of a patient with lower spastic paraparesis, dysarthria elements speech disorders, muscle hypotrophy, and inability to independent moving is presented. Differential diagnosis was performed between two diseases: amyotrophic lateral sclerosis and Strumpel's spastic familial paraplegia. The diagnosis was established after analyzing a set of data consisting of complaints, anamnesis, results of neurological examination, laboratory tests, instrumental research methods, including conclusions of needle electromyography and ultrasound examination of affected nerves and muscles despite the uncharacteristic symptoms of manifestation from spastic lower paraparesis: amyotrophic lateral sclerosis.
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作者简介
A. Zaytseva
Tver State Medical University; Regional Clinic Hospital
编辑信件的主要联系方式.
Email: kiralary@yandex.ru
ORCID iD: 0000-0002-2111-8919
SPIN 代码: 1375-4113
俄罗斯联邦, Tver; Tver
S. Medvedeva
Regional Clinic Hospital
Email: kiralary@yandex.ru
ORCID iD: 0000-0002-3729-0000
Candidate of Medical Sciences
俄罗斯联邦, TverYu. Gladkikh
Regional Clinic Hospital
Email: kiralary@yandex.ru
ORCID iD: 0009-0003-3808-7818
俄罗斯联邦, Tver
参考
- Siddique N., Siddique T. Amyotrophic lateral sclerosis overview. GeneReviews® [Internet], 2001 [Updated: 28 September 2023]. URL: https://www.ncbi.nlm.nih.gov/books/NBK1450/
- Wolfson C., Gauvin D.E., Ishola F. et al. Global prevalence and incidence of amyotrophic lateral sclerosis: a systematic review. Neurology. 2023; 101 (6): e613–e623. doi: 10.1212/WNL.0000000000207474
- Corcia P., Lunetta C., Vourc’h P. et al. Time for optimism in amyotrophic lateral sclerosis. Eur J Neurol. 2023; 30 (5): 1459–64. doi: 10.1111/ene.15738
- Мусаева Л.С., Завалишин И.А., Гулевская Т.С. Пирамидный синдром при боковом амиотрофическом склерозе: клинико-патоморфологическое исследование. Журнал неврологии и психиатрии им. С.С. Корсакова. 2003; 103 (5): 19–25 [Musaeva L., Zavalishin I., Gulevskaia T. Pyramidal syndrome in lateral amyotrophic sclerosis: clinico-morphological analysis. Zhurnal Nevrologii i Psikhiatrii Im. S S Korsakova. 2003; 103 (5): 19–25 (in Russ.)].
- Fink J.K. Progressive spastic paraparesis: hereditary spastic paraplegia and its relation to primary and amyotrophic lateral sclerosis. Semin Neurol. 2001; 21 (2): 199–207. doi: 10.1055/s-2001-15265
- Vander Stichele G., Durr A., Yoon G. et al. An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15. BMC Neurol. 2022; 22 (1): 115. doi: 10.1186/s12883-022-02595-4
- Meyyazhagan A., Kuchi Bhotla H., Pappuswamy M. et al. The puzzle of hereditary spastic paraplegia: from epidemiology to treatment. Int J Mol Sci. 2022; 23 (14): 7665. doi: 10.3390/ijms23147665
- Hedera P. Hereditary spastic paraplegia overview. GeneReviews® [Internet], 2000 [Updated 11 Feb 2021]. URL: https://www.ncbi.nlm.nih.gov/books/NBK1509/
- de Freitas J.L., Rezende Filho F.M., Sallum J.M.F. et al. Ophthalmological changes in hereditary spastic paraplegia and other genetic diseases with spastic paraplegia. J Neurol Sci. 2020; 409: 116620. doi: 10.1016/j.jns.2019.116620
- Sqalli Houssaini N., Belahsen F., Maaroufi M. et al. What is your diagnosis? J Neuroradiol. 2009; 36 (2): 107–8. doi: 10.1016/j.neurad.2008.10.005
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