Analysis of sensory function in Charcot-Marie-Tooth disease

Acta Neurologica Scandinavica

Volumn 99, Issue 5, 1999, Pages 291-296

  Ericson, UllaBritt ^a   Borg, K ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

Charcot Marie Tooths neuropathy; Hereditary motor and sensory neuropathies (HMSN); Somatosensory thresholds

Indexed keywords

ADULT; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; FOOT; HAND; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MALE; MYELINATED NERVE; NONMYELINATED NERVE; PAIN THRESHOLD; SENSORY DYSFUNCTION; THERMAL STIMULATION; VIBRATION SENSE;

EID: 0032958877     PISSN: 00016314     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0404.1999.tb00678.x     Document Type: Article

References (17)

1. DYCK PJ, CHANCE PF, LEBO RV, CARNEY JA. Hereditary Motor and Sensory Neuropathies. In Peripheral Neuropathy, edn 3. Philadelphia: W.B. Saunders, 1993;1094-136.
2. LUPSKI JR, GARCIA CA, PARRY GJ, PATEL PI. Charcot-Marie-Tooth Polyneuropathy Syndrome: Clinical, Electrophysiological and Genetics Aspects. In: APPEL S, ed. Current Neurology. Chicago: Mosby-Yearbook, 1991;1-25.
3. VANCE JM, NICOLSON GA, YAMAOKA LH. Linkage of Charcot-Marie-Tooth neuropathy type 1A to chromosome 17. Exp Neurol 1989;104:186-9.
4. RAYEMAKERS P, TIMMERMAN V, NELIS E et al. Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth disease type 1A. Nat Genet 1992;1:157-65.
5. LEBO RV, CHANCE PF, DYCK PJ et al. Chromosome 1 Charcot-Marie-Tooth syndrome (CMT1B) locus in FcyRII gene region. Hum Genet 1991;88:1-12.
6. FAIN PR, BARKER DF, CHANCE PF. Refined genetic mapping of the X-linked Charcot-Marie-Tooth neuropathy locus. Am J Hum Genet 1994;54:229-35.
7. IONASESCU VV, TROFATTER J, HAINES JL, IONASESCU R, SEARBY C. Heterogeniety in X-linked recessive Charcot-Marie-Tooth neuropathy. Am J Med Genet 1991;48:1075-83.
8. BEN OTHMANE K, HENTATI F, LENNON F et al. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Hum Mol Genet 1993;2:1625-8.
9. BEN OTHMANE K, MIDDLETON LT, LOPREST LJ et al. Localization of gene for autosomal dominant Charcot-Marie-Tooth type to chromosome 1p and evidence for genetic heterogeneity. Genomics 1993;17:370-5.
10. KWON JM, ELLIOT J, YEE WC et al. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q. Am J Hum Genet 1995;57:853-8.
11. HARDING AE, THOMAS PK. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain 1980;103:853-8.
12. BUCHTHAL F, BEHSE F. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography. Brain 1977;100:41-66.
13. HANSON P, DELTOMBE T. Preliminary study of large and small peripheral nerve fibers in Charcot-Marie-Tooth disease, type 1. Am J Phys Med Rehabil 1998;77:45-8.
14. HANSSON P, LINDBLOM U. LINDSTRÖM P. Graded assessment and classification of impaired temperature sensibility in patients with diabetic polyneuropathy. J Neurol Neurosurg Psychiatry 1991;54:527-30.
15. FRUHSTORFER H, LINDBLOM U, SCHMIDT WG. Method for quantitative estimation of thermal thresholds in patients. J Neurol Neurosurg Psychiatry 1976;39:1071-5.
16. GOLDBERG JM, LINDBLOM U. Standardized method of determining vibratory perception thresholds for diagnosis and screening in neurological investigation. J Neurol Neurosurg Psychiatry 1979;42:793-803.
17. LINDBLOM U, TEGNER R. Thermal sensitivity in uremic neuropathy. Acta Neurol Scand 1985;71:290-4.