OMIA 000715-9685 : Neuroaxonal dystrophy, generic in Felis catus
In other species: dog , horse , sheep , rabbit Possibly relevant human trait(s) and/or gene(s) (MIM number): 608507 (gene) Mendelian trait/disorder: unknown Considered a defect: yes Cross-species summary: Progressive ataxia, hypermetria, proprioceptive deficits, head incoordination and tremors.
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
|1996||Rodriguez, F., Delosmonteros, A.E., Morales, M., Herraez, P., Jaber, J.R., Fernandez, A. :|
|Neuroaxonal dystrophy in two siamese kitten littermates Veterinary Record 138:548-549, 1996. Pubmed reference: 8782363.|
|1993||Carmichael, K.P., Howerth, E.W., Oliver, J.E., Klappenbach, K. :|
|Neuroaxonal Dystrophy in a Group of Related Cats Journal of Veterinary Diagnostic Investigation 5:585-590, 1993. Pubmed reference: 8286459.|
- Created by Frank Nicholas on 06 Sep 2005