Classification and diagnosis of the inherited neuropathies
- PMID: 20142852
- PMCID: PMC2812746
- DOI: 10.4103/0972-2327.53075
Classification and diagnosis of the inherited neuropathies
Conflict of interest statement
Figures




Similar articles
-
Canine inherited motor and sensory neuropathies: an updated classification in 22 breeds and comparison to Charcot-Marie-Tooth disease.Vet J. 2011 Jun;188(3):274-85. doi: 10.1016/j.tvjl.2010.06.003. Epub 2010 Jul 16. Vet J. 2011. PMID: 20638305 Review.
-
A Brief Review of Inherited Neuropathies: A Perspective from Saudi Arabia.Brain Sci. 2025 Apr 17;15(4):403. doi: 10.3390/brainsci15040403. Brain Sci. 2025. PMID: 40309874 Free PMC article. Review.
-
Hereditary Sensory and Autonomic Neuropathies: Adding More to the Classification.Curr Neurol Neurosci Rep. 2019 Jun 20;19(8):52. doi: 10.1007/s11910-019-0974-3. Curr Neurol Neurosci Rep. 2019. PMID: 31222456 Review.
-
Progress in clinical neurosciences: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies.Can J Neurol Sci. 2001 Aug;28(3):199-214. doi: 10.1017/s0317167100001347. Can J Neurol Sci. 2001. PMID: 11513338 Review.
-
Carpal tunnel syndrome in inherited neuropathies: A retrospective survey.Muscle Nerve. 2018 Mar;57(3):388-394. doi: 10.1002/mus.25742. Epub 2017 Jul 21. Muscle Nerve. 2018. PMID: 28692128 Free PMC article.
Cited by
-
Congenital Insensitivity to Pain With Anhidrosis: A Case Report and Review of the Pertinent Literature.Cureus. 2022 Nov 2;14(11):e31019. doi: 10.7759/cureus.31019. eCollection 2022 Nov. Cureus. 2022. PMID: 36475157 Free PMC article.
-
Congenital insensitivity to pain and anhidrosis: a case report from South India.Indian J Dermatol. 2012 Nov;57(6):503. doi: 10.4103/0019-5154.103080. Indian J Dermatol. 2012. PMID: 23248377 Free PMC article.
-
Dominant aminoacyl-tRNA synthetase disorders: lessons learned from in vivo disease models.Front Neurosci. 2023 May 12;17:1182845. doi: 10.3389/fnins.2023.1182845. eCollection 2023. Front Neurosci. 2023. PMID: 37274211 Free PMC article. Review.
-
Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients.Sci Rep. 2021 Apr 19;11(1):8443. doi: 10.1038/s41598-021-86857-0. Sci Rep. 2021. PMID: 33875678 Free PMC article.
-
Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with GNB4 Mutations.Life (Basel). 2021 May 28;11(6):494. doi: 10.3390/life11060494. Life (Basel). 2021. PMID: 34071515 Free PMC article.
References
-
- Reilly MM. Sorting out the inherited neuropathies. Pract Neurol. 2007;7:93–105. - PubMed
-
- Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth's disease. Clin Genet. 1974;6:98–118. - PubMed
-
- Lewis RA, Sumner AJ. The electrodiagnostic distinctions between chronic familial and acquired demyelinative neuropathies. Neurology. 1982;32:592–6. - PubMed
-
- Lewis RA, Sumner AJ, Shy ME. Electrophysiological features of inherited demyelinating neuropathies: A reappraisal in the era of molecular diagnosis. Muscle Nerve. 2000;23:1472–87. - PubMed
-
- Dubourg O, Azzedine H, Verny C, Durosier G, Birouk N, Gouider R, et al. Autosomal-recessive forms of demyelinating Charcot- Marie- Tooth disease. Neuromolecular Med. 2006;8:75–86. - PubMed