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猎兔犬遗传性磷酸果糖激酶缺乏症。

Hereditary phosphofructokinase deficiency in wachtelhunds.

作者信息

Hillström Anna, Tvedten Harold, Rowe André, Giger Urs

机构信息

University Veterinary Hospital, Swedish University of Agricultural Sciences, Uppsala, Sweden.

出版信息

J Am Anim Hosp Assoc. 2011 Mar-Apr;47(2):145-50. doi: 10.5326/JAAHA-MS-5619. Epub 2011 Feb 10.

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.

摘要

在两只维希拉猎犬中诊断出遗传性磷酸果糖激酶(PFK)缺乏症,在另外三只患有运动不耐受、溶血性贫血和血红蛋白尿的相关维希拉猎犬中疑似存在该病症。鉴于仅有轻度贫血却伴有严重且持续的网织红细胞增多症,以及剧烈运动后出现血红蛋白尿,提示存在PFK缺乏症。红细胞PFK活性降低,同时2,3 - 二磷酸甘油酸浓度降低以及血红蛋白 - 氧亲和力升高,证实了诊断结果。在英国激飞猎犬、美国可卡犬、惠比特犬和混种犬中,PFK缺乏症是由肌肉型PFK M - PFK基因中的单个错义突变引起的;然而,这些PFK缺乏的维希拉猎犬并没有相同的PFK突变。

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本文引用的文献

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Hemolysis as a factor in clinical chemistry and hematology of the dog.
Vet Clin Pathol. 1989;18(3):58-68. doi: 10.1111/j.1939-165x.1989.tb00519.x.
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Molecular basis of canine muscle type phosphofructokinase deficiency.
J Biol Chem. 1996 Aug 16;271(33):20070-4. doi: 10.1074/jbc.271.33.20070.

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