Difference between revisions of "NEUROPATHY-DEMYELINATION"
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<br/>5. Weakness without atrophy. | <br/>5. Weakness without atrophy. | ||
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<br/>6. Heriditary disorders are diffuse & slowly progressive. | <br/>6. Heriditary disorders are diffuse & slowly progressive. | ||
Latest revision as of 02:29, 21 March 2023
SUMMARY
1. Inherited or inflammatory, acquired conditions are usually inflammatory.
2. Patchy or segmental in distribution, length-independent.
3. Involvement of the nerve roots is often seen with peripheral nerve trunks leading to proximal limb weakness (which is otherwise unusal in a neuropathy).
4. Rapid & complete recovery as the axons are spared.
5. Weakness without atrophy.
6. Heriditary disorders are diffuse & slowly progressive.
Reference(s)
Wilkinson, I., Furmedge, D. and Sinharay, R. (2017). Oxford handbook of clinical medicine. Oxford: Oxford University Press. Get it on Amazon.
Feather, A., Randall, D. and Waterhouse, M. (2020). Kumar And Clark’s Clinical Medicine. 10th ed. S.L.: Elsevier Health Sciences. Get it on Amazon.
Hannaman, R. A., Bullock, L., Hatchell, C. A., & Yoffe, M. (2016). Internal medicine review core curriculum, 2017-2018. CO Springs, CO: MedStudy.
Therapeutic Guidelines. Melbourne: Therapeutic Guidelines Limited. https://www.tg.org.au [Accessed 2021].
