OMIA:001197-9796 : Horner syndrome in Equus caballus (horse) |
In other species: dog , domestic cat , 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:001197-9796: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 1996 | Bacon, C.L., Davidson, H.J., Yvorchuk, K., Basaraba, R.J. : |
| Bilateral horners syndrome secondary to metastatic squamous cell carcinoma in a horse Equine Veterinary Journal 28:500-503, 1996. Pubmed reference: 9049502. |
Edit History
- Created by Frank Nicholas on 06 Sep 2005