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Peer-reviewed veterinary case report

Idiopathic low platelet counts in Cavalier King Charles Spaniels

By Singh, M K & Lamb, W A·Published in Australian veterinary journal·2005·Veterinary Specialist Centre, United Kingdom·View original on PubMed

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Original publication title: Idiopathic thrombocytopenia in Cavalier King Charles Spaniels.

Species:
dog

Plain-English summary

A group of Cavalier King Charles Spaniels (CKCS) in New South Wales was found to have a high rate of a blood condition called idiopathic macrothrombocytopenia, which means they had fewer platelets than normal. This condition often doesn't show any symptoms, but it can be inherited in a specific way. The study showed that CKCS had only about 32% of the platelet count compared to mixed breed dogs, and about 30% of them had larger platelets. Understanding this condition can help owners be aware of potential health issues in their CKCS.

People also search for: Cavalier King Charles Spaniel low platelet count · CKCS blood condition symptoms · dog macrothrombocytopenia treatment

Abstract

OBJECTIVE: To determine the prevalence of asymptomatic idiopathic macrothrombocytopenia in the population of Cavalier King Charles Spaniels (CKCS) in New South Wales (NSW) and to determine if it exhibits an autosomal recessive inheritance pattern. We also aimed to determine if significant differences existed when counting platelets manually, by auto analyser or by blood smear estimation in CKCS and mixed breed dogs. METHODS: Blood was collected from 172 dogs (152 CKCS and 20 mixed breed) and placed into sodium-citrate anticoagulant. Platelet counts were performed manually, by auto analyser and by blood smear estimates in CKCS and mixed breed dogs. Blood smears were also examined for platelet clumping and erythrocyte, leukocyte and platelet morphology. Pedigree analysis was performed to determine if an autosomal recessive inheritance pattern was supported. RESULTS: A statistically significant difference was found in platelet counts between CKCS and mixed breed dogs (P < 0.0001). CKCS had a platelet count that was 32% that of the controls (95% confidence interval, 28 to 37%). There was no significant difference between methods used to count platelets. Thirty percent of CKCS had macrothrombocytes. Pedigree analysis and examination of obtained and expected segregation ratios from 17 CKCS families supported an autosomal recessive pattern of Mendelian inheritance. CONCLUSIONS: A high prevalence of idiopathic macrothrombocytopenia exists in CKCS in NSW and automated or blood smear estimates are sufficient to count platelet numbers. Data supports an autosomal recessive inheritance pattern.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/16315671/