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1.
Aust Vet J ; 84(4): 122-8, 2006 Apr.
Article in English | MEDLINE | ID: mdl-16629191

ABSTRACT

OBJECTIVE: To determine the mode of inheritance of congenital proportionate dwarfism in Angus and Angus crossbred cattle, initially detected in two commercial beef herds in northern New South Wales. DESIGN: Matings of normal carrier sires to unrelated cows of diverse breeds, and of one carrier sire to his unaffected daughters. An unrelated Piedmontese bull was also mated to unaffected daughters of the carrier sires. PROCEDURE: Two carrier Angus bulls and nine unaffected daughters, all of whom were completely indistinguishable from normal animals, were purchased for controlled breeding studies under known nutritional and disease conditions. Affected and carrier individuals were examined for the presence of obvious chromosomal abnormalities. RESULTS: Angus dwarfism has been successfully reproduced under controlled experimental conditions over successive years using unrelated dams and is undoubtedly heritable. The high frequency of occurrence of affected individuals (23/61 = 0.38 +/- .06) among the progeny of matings of the Angus sires to unrelated females of diverse breeding is not compatible with recessive inheritance, because of the negligible frequency of proportionate dwarfism in the breeds of the dams. Both paternal and maternal transmission of the defect was demonstrated, so that imprinting in the strict sense of a gene that is only expressed when received from the male parent appears not to be involved. Tested individuals showed no evidence of gross chromosomal abnormality. Dominant autosomal inheritance with incomplete penetrance was indicated by the lack of expression of the defective gene in the two Angus sires and in three unaffected daughters who produced dwarf calves from matings to the Piedmontese bull. CONCLUSIONS: The mode of inheritance is that of a single autosomal dominant gene with a penetrance coefficient of 0.75 +/- 0.12, estimated from the observed incidence of 23/61 affected offspring of the two carrier Angus bulls mated to unrelated dams. Simple genetic models involving either (i) an unstable mutant which changes at high frequency to the expressed dominant dwarfing allele during gametogenesis, or (ii) a dominant allele with penetrance determined by an unlinked modifying locus, are shown to be compatible with the experimental data. Both models indicate that penetrance of the dwarfing gene may possibly be higher in matings involving carrier daughters of the two Angus bulls.


Subject(s)
Cattle Diseases/genetics , Crosses, Genetic , Dwarfism/veterinary , Genes, Dominant , Reproduction , Animals , Animals, Newborn , Breeding , Cattle , Dwarfism/genetics , Female , Genomic Imprinting , Male , Reproduction/genetics , Reproduction/physiology
2.
Aust Vet J ; 76(3): 199-202, 1998 Mar.
Article in English | MEDLINE | ID: mdl-9578757

ABSTRACT

OBJECTIVE: To describe the occurrence of chondrodysplasia in Australian Dexter cattle. DESIGN: A pathological and genetic case report. PROCEDURE: Congenital lethal chondrodysplasia was studied in two female Dexter foetuses aborted mid to late gestation. Clinicopathological findings including histological changes in limb bones, and analysis of pedigree information were evaluated. RESULTS: Characteristic features of congenital lethal chondrodysplasia (Dexter bulldog) include abortion, disproportionate dwarfism, a short vertebral column, marked micromelia, a relatively large head with retruded muzzle, cleft palate and protruding tongue and a large abdominal hernia. Histological changes in limb bones are consistent with failure of endochondral ossification. Dexter chondrodysplasia is considered to be inherited in an incompletely dominant manner with the homozygous form producing the congenital lethal condition. A preliminary minimum estimate of heterozygote frequency is 19% within the registered Australian Dexter herd, based on analysis of the contribution of three obligate heterozygotes whose semen has been widely used by artificial insemination in Australia. CONCLUSION: Dexter chondrodysplasia is present in Australian cattle and further cases of the homozygous form, congenital lethal chondrodysplasia, are likely to occur. RECOMMENDATION: It is requested that spleen and liver tissue from bulldog foetuses and blood from their parents be collected to assist research into Dexter chondrodysplasia.


Subject(s)
Abortion, Veterinary/pathology , Cattle Diseases/pathology , Chondrodysplasia Punctata, Rhizomelic/veterinary , Fetus/pathology , Animals , Cattle , Cattle Diseases/genetics , Chondrodysplasia Punctata, Rhizomelic/genetics , Chondrodysplasia Punctata, Rhizomelic/pathology , Female , Male , Pedigree , Pregnancy
5.
Vet Surg ; 19(3): 221-5, 1990.
Article in English | MEDLINE | ID: mdl-2349779

ABSTRACT

The left lateral hepatic lobe was removed in six dogs with a stapling instrument and in six dogs by blunt dissection and ligation. Both techniques were safe and effective. Lobectomy by dissection and ligation was slower and less complete than by stapling. Major intraoperative or postoperative hemorrhage did not occur with either method. Serum chemistry values were elevated after surgery in all dogs but did not differ significantly between treatment groups. Microscopic hemorrhage, necrosis, and inflammation of the lobectomy site were more pronounced after dissection and ligation than stapling.


Subject(s)
Dogs/surgery , Hepatectomy/veterinary , Surgical Staplers/veterinary , Animals , Ligation/veterinary
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