Amyotrophic lateral sclerosis with damage to the upper motor neuron (clinical case)

封面

如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅或者付费存取

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.

全文:

受限制的访问

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, Tver

Yu. Gladkikh

Regional Clinic Hospital

Email: kiralary@yandex.ru
ORCID iD: 0009-0003-3808-7818
俄罗斯联邦, Tver

参考

  1. Siddique N., Siddique T. Amyotrophic lateral sclerosis overview. GeneReviews® [Internet], 2001 [Updated: 28 September 2023]. URL: https://www.ncbi.nlm.nih.gov/books/NBK1450/
  2. 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
  3. 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
  4. 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.)].
  5. 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
  6. 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
  7. 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
  8. Hedera P. Hereditary spastic paraplegia overview. GeneReviews® [Internet], 2000 [Updated 11 Feb 2021]. URL: https://www.ncbi.nlm.nih.gov/books/NBK1509/
  9. 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
  10. 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

补充文件

附件文件
动作
1. JATS XML

版权所有 © Russkiy Vrach Publishing House, 2025