Hereditary Phosphofructokinase Deficiency in Wachtelhunds

Author:

Hillström Anna1,Tvedten Harold1,Rowe André1,Giger Urs1

Affiliation:

1. University Veterinary Hospital, Swedish University of Agricultural Sciences (SLU), Uppsala, Sweden (A.H., H.T.); Strömsholm Referral Animal Hospital, Strömsholm, Sweden (A.R., A.H., H.T.); and Section of Medical Genetics, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA (U.G.).

Abstract

Hereditary phosphofructokinase (PFK) deficiency was diagnosed in two Wachtelhund dogs and suspected in three related Wachtelhund dogs with exercise intolerance, hemolytic anemia, and pigmenturia. Severe, persistent reticulocytosis in light of only mild anemia together with hemoglobinuria after strenuous exercise suggested PFK deficiency. Low erythrocyte PFK activity together with low 2,3-diphosphoglycerate concentrations and a high hemoglobin-oxygen affinity confirmed the diagnosis. The PFK deficiency is due to a single missense mutation in the muscle-type PFK M-PFK gene in English springer and American cocker spaniels, whippets, and mixed-breed dogs; however, these PFK-deficient Wachtelhunds do not have the same PFK mutation.

Publisher

American Animal Hospital Association

Subject

Small Animals

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