OMIA:000527-9615 : Hypomyelinogenesis, congenital in Canis lupus familiaris (dog) |
In other species: pig , taurine cattle , sheep
Categories: Nervous system phene
Links to MONDO diseases: No links.
Mendelian trait/disorder: unknown
Considered a defect: yes
Cross-species summary: Congenital deficiency of myelin, especially in the cerebellum and brainstem; includes failure of formation of myelin, plus incomplete and delayed myelination of axons. Clinical signs include inability to rise, and severe muscle tremor with periods of spasticity. Also known as oligodendroglial dysplasia.
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. (2014). OMIA:000527-9615: Online Mendelian Inheritance in Animals (OMIA) [dataset]. https://omia.org/. https://doi.org/10.25910/2AMR-PV70
Reference
| 2006 | Morrison, J.P., Schatzberg, S.J., De Lahunta, A., Ross, J.T., Bookbinder, P., Summers, B.A. : |
| Oligodendroglial dysplasia in two bullmastiff dogs. Vet Pathol 43:29-35, 2006. Pubmed reference: 16407484. DOI: 10.1354/vp.43-1-29. |
Edit History
- Created by Frank Nicholas on 17 Sep 2014