Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/132419
Title: Feline hypertrophic cardiomyopathy - Bibliographic Review and Clinical Cases
Authors: Peñate López, Elsa María
Director: Déniz Suárez, María Soraya 
Reina Doreste, Yamir 
UNESCO Clasification: 310907 Patología
310904 Medicina interna
Keywords: Cardiomyopathy
hypertrophy
feline
ventricle
atrium, et al
Issue Date: 2024
Abstract: This paper presents a review of the literature on the most commonly observed cardiac disease in the cat. Feline hypertrophic cardiomyopathy (or HCM) is a primary heart muscle disease characterised by concentric left ventricular hypertrophy usually of unknown cause. The occurrence of mutations in certain genes raises the suspicion of a possible genetic origin in certain cat breeds. There is a wide variety of phenotypic manifestations and clinical pictures depending on the numerous particular features of its pathophysiology. There are a wide range of clinical signs related to feline HCM depending on the disease stage: from vague signs of malaise to severe respiratory signs (congestive heart failure) or pain (arterial thromboembolism). Although rare, cat owners should be aware of sudden death due to malignant ventricular arrhythmias. Many cats affected with HCM may remain asymptomatic. Echocardiography is widely recognised as the “gold standard” for diagnosing HCM, although other tests can help classify the disease and determine prognosis. Treatment of HCM focuses on reducing the effects of hypertrophy and diastolic dysfunction. The choice of therapy will depend on the stage of the patient´s disease. Feline HCM closely resembles human HCM and is suggested as translational animal model for the human disease.
Department: Departamento de Patología Animal, Producción Animal, Bromatología y Tecnología de Los Alimentos
Faculty: Facultad de Veterinaria
Degree: Grado en Veterinaria
URI: http://hdl.handle.net/10553/132419
Appears in Collections:Trabajo final de grado

En el caso de que no encuentre el documento puede ser debido a que el centro o las/os autoras/es no autorizan su publicación. Si tiene verdadero interés en el contenido del mismo, puede dirigirse al director/a o directores/as del trabajo cuyos datos encontrará más arriba.

Show full item record

Google ScholarTM

Check


Share



Export metadata



Items in accedaCRIS are protected by copyright, with all rights reserved, unless otherwise indicated.