Charcot-Marie-Tooth disease: Inherited neuropathies revisited

Veterinary Journal

Volumn 188, Issue 3, 2011, Pages 254-255

  Matiasek, Kaspar ^a   Drögemüller, Cord ^b  

^a UNIVERSITY OF MUNICH   (Germany)

^b UNIVERSITY OF BERN   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CATTLE; DISEASE COURSE; DOG; EDITORIAL; GENE MUTATION; GENOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; MUSCLE ATROPHY; NERVE BIOPSY; NONHUMAN; PHENOTYPIC VARIATION; SINGLE NUCLEOTIDE POLYMORPHISM;

ANIMALS; CHARCOT-MARIE-TOOTH DISEASE; DISEASE MODELS, ANIMAL; DOG DISEASES; DOGS; HEREDITARY SENSORY AND MOTOR NEUROPATHY; HUMANS; MUTATION;

EID: 79955862629     PISSN: 10900233     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tvjl.2011.03.002     Document Type: Editorial

References (16)

1. Baranowska I., Jaderlund K.H., Nennesmo I., Holmqvist E., Heidrich N., Larsson N.G., Andersson G., Wagner E.G., Hedhammar A., Wibom R., Andersson L. Sensory ataxic neuropathy in golden retriever dogs is caused by a deletion in the mitochondrial tRNATyr gene. PLoS Genetic 2009, 5:e1000499.
2. Charcot J.M., Marie P. Sure une forme particulière d́atrophie musculaire progressive, souvent familiale, débutant par les pieds et les jambes et atteignant plus tard les mains. Revue Médicinale 1886, 6:97-138.
3. Drogemuller C., Becker D., Kessler B., Kemter E., Tetens J., Jurina K., Jaderlund K.H., Flagstad A., Perloski M., Lindblad-Toh K., Matiasek K. A deletion in the N-myc downstream regulated gene 1 (NDRG1) gene in Greyhounds with polyneuropathy. PLoS ONE 2010, 5:e11258.
4. Ekenstedt, K.J., Drögemüller, C., Minor, K.M., Shelton, G.D., Leeb, T., Patterson, N., Mickelson, J., 2010. Whole-genome association analysis reveals two loci strongly associated with Leonberger polyneuropathy. In: 5th International Conference on Advances in Canine and Feline Genomics and Inherited Diseases. Baltimore, p. 32.
5. Granger N. Canine inherited motor and sensory neuropathies: an updated classification in 22 breeds and comparison to Charcot-Marie-Tooth disease. The Veterinary Journal 2011, 188:274-285.
6. Karlsson E.K., Baranowska I., Wade C.M., Salmon Hillbertz N.H., Zody M.C., Anderson N., Biagi T.M., Patterson N., Pielberg G.R., Kulbokas E.J., Comstock K.E., Keller E.T., Mesirov J.P., von Euler H., Kampe O., Hedhammar A., Lander E.S., Andersson G., Andersson L., Lindblad-Toh K. Efficient mapping of Mendelian traits in dogs through genome-wide association. Nature Genetics 2007, 39:1321-1328.
7. Keller M.P., Chance P.F. Inherited neuropathies: from gene to disease. Brain Pathology 1999, 9:327-341.
8. Nicholas F.W. Online Mendelian Inheritance in Animals (OMIA): a comparative knowledgebase of genetic disorders and other familial traits in non-laboratory animals. Nucleic Acids Research 2003, 31:275-277.
9. Ostrander E.A., Galibert F., Patterson D.F. Canine genetics comes of age. Trends in Genetics 2000, 16:117-124.
10. Pareyson D., Marchesi C., Salsano E. Hereditary predominantly motor neuropathies. Current Opinion in Neurology 2009, 22:451-459.
11. Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth's disease. Clinical Genetics 1974, 6:98-118.
12. Syring C., Drogemuller C., Oevermann A., Pfister P., Henke D., Muller S., Solkner J., Leeb T., Meylan M. Degenerative axonopathy in a Tyrolean grey calf. Journal of Veterinary Internal Medicine 2010, 24:1519-1523.
13. Tooth, H.H., 1886. The peroneal type of progressive muscular atrophy. In: A Thesis for the Degree of Doctor of Medicine in the University of Cambridge, H. K. Lewis, London, p. 43.
14. van Doorn P.A., Merkies I.S. How to assess new drugs for neuropathies: advances in trial design and methodology. Current Opinion in Neurology 2008, 21:519-526.
15. Vance J.M., Nicholson G.A., Yamaoka L.H., Stajich J., Stewart C.S., Speer M.C., Hung W.Y., Roses A.D., Barker D., Pericak-Vance M.A. Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17. Experimental Neurology 1989, 104:186-189.
16. Vanhaesebrouck A.E., Couturier J., Cauzinille L., Mizisin A.P., Shelton G.D., Granger N. Demyelinating polyneuropathy with focally folded myelin sheaths in a family of Miniature Schnauzer dogs. Journal of Neurological Science 2008, 275:100-105.