OMIA:000478-9796 : Holoprosencephaly in Equus caballus
Categories: Craniofacial phene
Possibly relevant human trait(s) and/or gene(s)s (MIM numbers): 236100 (trait) , 157170 (trait) , 142945 (trait) , 142946 (trait) , 609637 (trait) , 605934 (trait) , 610828 (trait) , 609408 (trait) , 610829 (trait) , 614226 (trait)
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Developmental failure of cleavage of the forebrain (prosencephalon); with a deficit in midline facial development, and with cyclopia (see MIA 000249) in the severe form.
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.
|2022||Henker, L.C., Lorenzett, M.P., Piva, M.M., Wronski, J.G., de Andrade, D.G.A., Borges, A.S., Driemeier, D., Oliveira-Filho, J.P., Pavarini, S.P. :|
|Alobar holoprosencephaly in an aborted American Quarter Horse fetus. J Equine Vet Sci 112:103898, 2022. Pubmed reference: 35150851 . DOI: 10.1016/j.jevs.2022.103898.|
|2005||Koch, T., Loretti, A., de Lahunta, A., Kendall, A., Russell, D., Bienzle, D. :|
|Semilobar holoprosencephaly in a Morgan horse. J Vet Intern Med 19:367-72, 2005. Pubmed reference: 15954555 .|
- Created by Frank Nicholas on 18 Sep 2005
- Changed by Imke Tammen2 on 12 Feb 2023