OMIA:001197-9685 : Horner syndrome in Felis catus (domestic cat) |
In other species: dog , horse , taurine cattle
Categories: Nervous system phene
Possibly relevant human trait(s) and/or gene(s) (MIM number): 143000 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Due to damage to the sympathetic nerves of the face - characterised by miosis (constriction of the pupil), ptosis (drooping of the upper eyelid), and anhidrosis (absence of sweating of the face)
Genetic engineering:
Unknown
Have human generated variants been created, e.g. through genetic engineering and gene editing
Cite this entry
Nicholas, F. W., Tammen, I., & Sydney Informatics Hub. (2005). OMIA:001197-9685: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
References
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.
| 2004 | Krotscheck, U., Kunze, CP., Bergman, RL. : |
| What is your diagnosis? Horner syndrome. J Am Vet Med Assoc 225:1337-8, 2004. Pubmed reference: 15552304. | |
| 1996 | Holland, C.T. : |
| Horners syndrome and ipsilateral laryngeal hemiplegia in three cats Journal of Small Animal Practice 37:442-446, 1996. Pubmed reference: 8887205. | |
| 1995 | Shell, L.G. : |
| Horners syndrome Feline Practice 23:28-29, 1995. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005