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1.
J Vet Cardiol ; 27: 10-22, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31881369

RESUMO

INTRODUCTION: To describe unexpected sudden cardiac death (SCD) in young Leonbergers (<3 years) and to review the circumstances before death and necropsy findings; to prospectively evaluate the presence of possible arrhythmias in young Leonbergers; and to examine pedigrees for determining potential modes of inheritance. ANIMALS: Postmortem evaluations included 21 Leonbergers. Clinical evaluation consisted of 46 apparently healthy Leonbergers with and without a close family history of SCD. MATERIALS AND METHODS: Necropsy reports were reviewed retrospectively. Prospective clinical evaluation included physical examination, 5-min electrocardiogram, 24-h Holter, echocardiography, and laboratory tests. Pedigree data were examined for mode of inheritance. RESULTS: Based on necropsy reports, SCD occurred at a median age of 12 months (range, 2.0-32.0 months) without any previous clinical signs and usually in rest. No evidence of structural cardiac disease was found; arrhythmia-related death was suspected. Clinical evaluation and 24-h Holter showed ventricular arrhythmia (VA) in 14 apparently healthy Leonbergers (median age, 18 months; range, 12-42 months). Severity of VA varied from infrequent couplets/triplets to frequent complexity (couplets, triplets, nonsustained ventricular tachycardias,VTs) characterized by polymorphology. During follow-up, two dogs with polymorphic VT died. Although breed specificity and high prevalence indicate a heritable disease, based on available pedigree data, the mode of inheritance could not be determined. CONCLUSIONS: Sudden cardiac death in young Leonbergers is associated with malignant VA characterized by complexity and polymorphic nature. Diagnosis is based on 24-h Holter monitoring. Pedigree analysis suggests that the arrhythmia is familial.


Assuntos
Arritmias Cardíacas/veterinária , Morte Súbita Cardíaca/veterinária , Doenças do Cão/diagnóstico , Animais , Arritmias Cardíacas/diagnóstico , Arritmias Cardíacas/genética , Doenças do Cão/genética , Cães , Eletrocardiografia/veterinária , Eletrocardiografia Ambulatorial/veterinária , Masculino , Linhagem
2.
J Small Anim Pract ; 52(6): 319-24, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21627660

RESUMO

This case series describes four cases of concomitant dermoid sinus and spina bifida in a Chinese crested dog, two Swedish vallhunds and a Burmese cat. The diagnosis was confirmed by computed tomography, computed tomography fistulography and pathology. Two dogs that showed abnormalities during neurological examination underwent magnetic resonance imaging. One of them had imaging findings interpreted as syringohydromyelia. All the dogs underwent surgery and the outcome was considered good in all the cases. Based on clinical and pathological examination as well as diagnostic imaging findings, two of the dermoid sinuses were classified as type IV, and two of them showed a previously unreported type of dermoid sinus. This new type is suggested here as type VI.


Assuntos
Doenças do Gato/diagnóstico , Doenças do Cão/diagnóstico , Espinha Bífida Oculta/veterinária , Disrafismo Espinal/veterinária , Animais , Gatos , Doenças do Cão/cirurgia , Cães , Feminino , Imageamento por Ressonância Magnética/veterinária , Masculino , Espinha Bífida Oculta/diagnóstico , Espinha Bífida Oculta/cirurgia , Disrafismo Espinal/diagnóstico , Disrafismo Espinal/cirurgia , Tomografia Computadorizada por Raios X/veterinária , Resultado do Tratamento
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