OMIA 002419-9940 : Daft lamb syndrome, Type II in Ovis aries
Mendelian trait/disorder: unknown Mode of inheritance: Probably Autosomal Recessive Considered a defect: yes Species-specific name: This condition is clinically indistinguishable from daft lamb disease (OMIA 000177-9940 : Cerebellar cortical atrophy in Ovis aries), but differs by the absence of noticeable changes to the cerebellum or other parts of the CNS. In addition to typical congenital neurological clinical science, skeletal fragility and a progressive myopathy was noted. Breed: Border Leicester.
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.
|1978||Bradley, R. :|
|Hereditary "daft lamb" disease of Border Leicester sheep: the ultrastructural pathology of the skeletal muscles. J Pathol 125:205-12, 1978. Pubmed reference: 722402. DOI: 10.1002/path.1711250406.|
|Bradley, R., Terlecki, S. :|
|Muscle lesions in a hereditary disease of lambs (`daft lamb disease') Neuropathology and Applied Neurobiology 4:237, 1978.|
|Terlecki, S., Richardson, C., Bradley, R., Buntain, D., Young, G.B., Pampiglione, G. :|
|A congenital disease of lambs clinically similar to 'inherited cerebellar cortical atrophy' (daft lamb disease). British Veterinary Journal 134:299-307, 1978. DOI: 10.1016/S0007-1935(17)33431-0.|
- Created by Imke Tammen2 on 10 Sep 2021
- Changed by Imke Tammen2 on 10 Sep 2021