Evidence of Inheritance of Intrahepatic Portosystemic Shunts in Irish Wolfhounds

Background: The etiogenesis of congenital portosystemic shunt in dogs is not understood. In Irish Wolfhounds, intrahepatic portosystemic shunt (IHPSS) is thought to be hereditary, but the mode of inheritance is unknown. Objectives: To document the genetic background and investigate the potential mod...

Full description

Saved in:
Bibliographic Details
Published inJournal of veterinary internal medicine Vol. 23; no. 4; pp. 950 - 952
Main Authors Steenbeek, F.G. van, Leegwater, P.A.J, Sluijs, F.J. van, Heuven, H.C.M, Rothuizen, J
Format Journal Article
LanguageEnglish
Published Malden, USA Blackwell Publishing Inc 01.07.2009
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Background: The etiogenesis of congenital portosystemic shunt in dogs is not understood. In Irish Wolfhounds, intrahepatic portosystemic shunt (IHPSS) is thought to be hereditary, but the mode of inheritance is unknown. Objectives: To document the genetic background and investigate the potential mode of inheritance of IHPSS in Irish Wolfhounds. Animals: Three mature, privately owned, affected siblings and their progeny produced in 2 litters. Methods: Prospective, observational study. Two test matings of 1 affected sire with 2 of his affected sisters were used to determine the inheritance pattern. Affection status was determined by measuring venous blood ammonia concentrations, detection of the shunt by ultrasonography and confirmation during surgical attenuation of the intrahepatic shunting vessel. Results: In 1 litter of 5 pups all had an IHPSS. In the other litter 5 of 11 pups were affected. Both left‐ and right‐sided shunts occurred in both litters. No sex predisposition was evident among affected dogs. Conclusions and Clinical Importance: Our results show that IHPSS in Irish Wolfhounds is a familial disorder that is likely genetic. It is unlikely that the mode of inheritance is monogenic. A digenic, triallelic trait could explain the observed occurrence of IHPSS but other modes of inheritance cannot be excluded.
Bibliography:ark:/67375/WNG-P28DD82N-T
ArticleID:JVIM319
istex:61A7ABDD4B2579CE13ABD436E667906AF247D951
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0891-6640
1939-1676
DOI:10.1111/j.1939-1676.2009.0319.x