Literature DB >> 3750776

Inherited congenital myoclonus of polled Hereford calves (so-called neuraxial oedema): a clinical, pathological and biochemical study.

P A Harper, P J Healy, J A Dennis.   

Abstract

Thirty-four newborn polled Hereford and polled Hereford cross calves affected with a condition previously described as neuraxial oedema and six normal calves were examined. None of the affected calves were seen to stand after birth and when first examined the calves were in lateral recumbency, with extension and crossing of the hindlimbs. All the affected calves were bright and alert, could lift their heads and apparently could see and hear. When the calves were encouraged to stand spontaneous and stimulus-responsive myoclonic extensor spasms, with whole body rigidity, were consistently observed. Thirty-two of the affected calves had macroscopic lesions in the coxae. No significant pathological or biochemical lesions were observed in the central nervous system of any of the calves. The water content of the cerebellum did not differ between normal and affected calves. As oedema of the central nervous system is not a feature of this condition it is more appropriate to describe it as inherited congenital myoclonus.

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Year:  1986        PMID: 3750776     DOI: 10.1136/vr.119.3.59

Source DB:  PubMed          Journal:  Vet Rec        ISSN: 0042-4900            Impact factor:   2.695


  4 in total

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Authors:  J D Baird; Z W Wojcinski; A P Wise; M A Godkin
Journal:  Can Vet J       Date:  1987-08       Impact factor: 1.008

2.  Lafora disease as a cause of visually exacerbated myoclonic attacks in a dog.

Authors:  Aubrey A Webb; Chantal McMillan; Cheryl L Cullen; Sarah E Boston; Julie Turnbull; Berge A Minassian
Journal:  Can Vet J       Date:  2009-09       Impact factor: 1.008

Review 3.  Virus-induced congenital malformations in cattle.

Authors:  Jørgen S Agerholm; Marion Hewicker-Trautwein; Klaas Peperkamp; Peter A Windsor
Journal:  Acta Vet Scand       Date:  2015-09-24       Impact factor: 1.695

4.  Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 gene.

Authors:  Jennifer L Gill; Deborah Capper; Jean-François Vanbellinghen; Seo-Kyung Chung; Robert J Higgins; Mark I Rees; G Diane Shelton; Robert J Harvey
Journal:  Neurobiol Dis       Date:  2011-03-17       Impact factor: 5.996

  4 in total

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