OMIA:000715-9685 : Neuroaxonal dystrophy, generic in Felis catus (domestic cat)
Categories: Nervous system phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 608507 (gene)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Progressive ataxia, hypermetria, proprioceptive deficits, head incoordination and tremors.
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
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