TY - JOUR
T1 - Inheritance of rupture of the cranial cruciate ligament in Newfoundlands
AU - Wilke, Vicki L.
AU - Conzemius, Michael G.
AU - Kinghorn, Brian P.
AU - Macrossan, Paula E.
AU - Cai, Weiguo
AU - Rothschild, Max F.
N1 - Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2006/1/1
Y1 - 2006/1/1
N2 - Objective - To determine prevalence, level of inbreeding, heritability, and mode of inheritance for rupture of the cranial cruciate ligament (RCCL) in Newfoundlands. Design - Retrospective and recruitment study. Animals-574 client-owned Newfoundlands. Procedure - Medical records from January 1, 1996, to December 31, 2002, were evaluated for prevalence of RCCL. A pedigree was constructed by use of recruited Newfoundlands with RCCL status based on results of veterinary examination; level of inbreeding, heritability, and mode of inheritance were calculated. Results - Hospital prevalence for RCCL was 22%; dogs in the pedigree from the recruitment study had a mean level of inbreeding of 1.19 × 10-4, heritability of 0.27, and a possible recessive mode of inheritance with 51% penetrance for RCCL. Conclusions and Clinical Relevance - Identification of a genetic basis for RCCL in Newfoundlands provided evidence that investigators can now focus on developing methods to identify carriers to reduce the prevalence of RCCL.
AB - Objective - To determine prevalence, level of inbreeding, heritability, and mode of inheritance for rupture of the cranial cruciate ligament (RCCL) in Newfoundlands. Design - Retrospective and recruitment study. Animals-574 client-owned Newfoundlands. Procedure - Medical records from January 1, 1996, to December 31, 2002, were evaluated for prevalence of RCCL. A pedigree was constructed by use of recruited Newfoundlands with RCCL status based on results of veterinary examination; level of inbreeding, heritability, and mode of inheritance were calculated. Results - Hospital prevalence for RCCL was 22%; dogs in the pedigree from the recruitment study had a mean level of inbreeding of 1.19 × 10-4, heritability of 0.27, and a possible recessive mode of inheritance with 51% penetrance for RCCL. Conclusions and Clinical Relevance - Identification of a genetic basis for RCCL in Newfoundlands provided evidence that investigators can now focus on developing methods to identify carriers to reduce the prevalence of RCCL.
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U2 - 10.2460/javma.228.1.61
DO - 10.2460/javma.228.1.61
M3 - Article
C2 - 16426167
AN - SCOPUS:29844434591
VL - 228
SP - 61
EP - 64
JO - Journal of the American Veterinary Medical Association
JF - Journal of the American Veterinary Medical Association
SN - 0003-1488
IS - 1
ER -