Charcot-Marie-Tooth Disease: Extensive Cranial Nerve Involvement on CT and MR Imaging

American Journal of Neuroradiology

Volumn 25, Issue 3, 2004, Pages 494-497

  Aho, Todd R ^a   Wallace, Robert C ^a   Pitt, Alan M ^a   Sivakumar, Kumaraswamy ^a  

^a BARROW NEUROLOGICAL INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BONE RADIOGRAPHY; CASE REPORT; COMPUTER ASSISTED TOMOGRAPHY; CONTRAST ENHANCEMENT; CONTRAST RADIOGRAPHY; CRANIAL NEUROPATHY; ELECTROPHYSIOLOGY; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LUMBOSACRAL SPINE; MALE; MUSCLE WEAKNESS; NERVE COMPRESSION; NERVE ROOT; NUCLEAR MAGNETIC RESONANCE IMAGING; SKULL BASE;

CHARCOT-MARIE-TOOTH DISEASE; CHROMOSOME DELETION; COCHLEAR NERVE; CRANIAL NERVE DISEASES; DEAFNESS; FACIAL NERVE; HUMANS; HYPERTROPHY; MAGNETIC RESONANCE IMAGING; MALE; MASTOID; MEMBRANE PROTEINS; MIDDLE AGED; PEDIGREE; TOMOGRAPHY, X-RAY COMPUTED; TRIGEMINAL NERVE; TRIGEMINAL NEURALGIA;

EID: 1642292627     PISSN: 01956108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (15)

1. Bird TD. Hereditary motor-sensory neuropathies: Charcot-Marie-Tooth syndrome. Neurol Clin 1989;7:9-23
2. Kremenitzer M, Ager PJ, Zingesser LH. Myelographic evidence for nerve enlargement in a case of Charcot-Marie-Tooth disease. Neuroradiology 1976;11:165-167
3. Morano JU, Russell WF. Nerve root enlargement in Charcot-Marie-Tooth disease: CT appearance. Radiology 1986;161:784
4. 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
5. 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
6. Sambuughin N, de Bantel A, McWilliams S, Sivakumar K. Deafness and CMT disease associated with a novel four amino acid deletion in the PMP22 gene. Neurology 2003;60:506-508
7. Dyck PJ, Chance P, Lebo R, et al. Hereditary motor and sensory neuropathies. In: Dyck PJ, Thomas PK, et al, eds. Peripheral Neuropathy, 3rd ed. Philadelphia: WB Saunders, 1993:1094-1136
8. Testa D, Milanese C, Mantia L, et al. Familial trigeminal neuralgia in Charcot-Marie-Tooth disease. J Neurol 1981;25:283-287
9. Shizuka M, Ikeda Y, Watanabe M, et al. A novel mutation of the myelin P(o) gene segregating Charcot-Marie-Tooth disease type 1B manifesting as trigeminal nerve thickening. J Neurol Neurosurg Psychiatry 1999;67:250-251
10. Waddy HM, Misra VP, King RHM, et al. Focal cranial nerve involvement in chronic inflammatory demyelinating polyneuropathy: clinical and MRI evidence of peripheral and central lesions. J Neurol 1989;236:400-405
11. Duarte J, Martinez AC, Rodriguez F, et al. Hypertrophy of multiple cranial nerves and spinal roots in chronic inflammatory demyelinating neuropathy. J Neurol Neurosurg Psychiatry 1999;67:685-687
12. Schady W, Goulding PJ, Lecky BRF, et al. Massive nerve root enlargement in chronic inflammatory demyelinating polyneuropathy. J Neurol Neurosurg Psychiatry 1996;61:636-640
13. Roos KL, Pascuzzi RM, Dunn DW. Neurofibromatosis, Charcot-Marie-Tooth disease, or both? Neurofibromatosis 1989;2:238-243
14. Antoine JC, Baril A, Guettier C, et al. Unusual amyloid polyneuropathy with predominant lumbosacral nerve roots and plexus involvement. Neurology 1991;41:206-208
15. O'Brien TJ, McKelvie PA, Vrodos N. Bilateral trigeminal amyloidoma: an unusual case of trigeminal neuropathy with a review of the literature-case report. J Neurosurg 1994;81:780-783