OMIA:000527-9615 : Hypomyelinogenesis, congenital in Canis lupus familiaris (dog)

In other species: pig , taurine cattle , sheep

Categories: Nervous system phene

Single-gene trait/disorder: unknown

Disease-related: 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.

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.

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  • Created by Frank Nicholas on 17 Sep 2014