Charcot-Marie-Tooth disease: extensive cranial nerve involvement on CT and MR imaging
- PMID: 15037479
- PMCID: PMC8158541
Charcot-Marie-Tooth disease: extensive cranial nerve involvement on CT and MR imaging
Abstract
We report a case of genetically verified Charcot-Marie-Tooth disease in which the patient had cranial nerve symptoms. CT and MR imaging demonstrated enlargement of several cranial nerves, as well as their skull-base foramina, with faint contrast material enhancement identified.
Figures
References
-
- Bird TD. Hereditary motor-sensory neuropathies: Charcot-Marie-Tooth syndrome. Neurol Clin 1989;7:9–23 - PubMed
-
- Kremenitzer M, Ager PJ, Zingesser LH. Myelographic evidence for nerve enlargement in a case of Charcot-Marie-Tooth disease. Neuroradiology 1976;11:165–167 - PubMed
-
- Morano JU, Russell WF. Nerve root enlargement in Charcot-Marie-Tooth disease: CT appearance. Radiology 1986;161:784. - PubMed
-
- Rosen SA, Wang H, Cornblath DR, et al. Compression syndromes due to hypertrophic nerve roots in hereditary motor sensory neuropathy I. Neurology 1989;39:1173–1177 - PubMed
-
- Choi SK, Bowers RP, Buckthal PE. MR imaging in hypertrophic neuropathy: a case of hereditary motor and sensory neuropathy, type I (Charcot-Marie-Tooth). Clin Imag 1990;14:204–207 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical