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Peer-reviewed veterinary case report

Border Collie puppy with trapped neutrophil syndrome and infections

By Mizukami, Keijiro et al.Ā·Published in The Journal of veterinary medical scienceĀ·2012Ā·Department of Veterinary Medicine, JapanĀ·View original on PubMed →

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Original publication title: Trapped neutrophil syndrome in a Border Collie dog: clinical, clinico-pathologic, and molecular findings.

Species:
dog

Plain-English summary

A 10-week-old male Border Collie was brought in for recurrent infections and other health issues. A blood test showed he had very low white blood cell counts, indicating a genetic condition called trapped neutrophil syndrome (TNS), which affects his immune system. Genetic testing confirmed he inherited the condition from both parents, who were carriers. This case highlights the importance of genetic testing for early diagnosis of TNS in dogs, which can help in managing the condition and preventing future cases.

People also search for: Border Collie recurrent infections Ā· trapped neutrophil syndrome in dogs Ā· dog genetic testing for immune issues

Abstract

Trapped neutrophil syndrome (TNS) is an autosomal recessive inherited neutropenia known in Border Collies since the 1990's. Recently, the causative mutation has been identified in the canine VPS13B gene and a DNA-based diagnosis has now become available. The present paper describes clinical and clinico-pathologic findings in a Border Collie with TNS that was molecularly diagnosed for the first time in Japan. In a 10-week-old male Border Collie with microgenesis and symptoms related to recurrent infections, a hematological examination revealed severe leukopenia due to neutropenia, suggesting the dog to be affected by inherited neutropenic immunodeficiency. Direct DNA sequencing demonstrated that the dog was homozygous for the causative mutation of TNS and both its parents were heterozygous carriers. In addition, a simple and rapid polymerase chain reaction-based length polymorphism analysis coupled with microchip electrophoresis was developed for the genotyping of TNS. This assay could discriminate clearly all genotypes, suggesting that it was suitable for both individual diagnosis and large-scale surveys for prevention.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/22240985/