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Foi avaliado o tratamento homeopático de um felino com doença renal policística, moléstia hereditária muito comum na espécie felina. Por ser progressiva, o prognóstico depende do estágio de evolução da doença renal crônica, da resposta do felino ao tratamento inicial e do desejo do tutor em dar continuidade ao tratamento. A observação teve duração de 9 (nove) meses e a avaliação dos resultados foi realizada com o emprego de exame clínico e de exames complementares como imagens ultrassonográficas e exames laboratoriais. A terapia foi composta por medicamento homeopático constitucional Phosphorus 30CH e episódico Kresolum 6CH associado à introdução de dieta renal (ração seca adjuvante). O medicamento homeopático não provocou eventos adversos no animal. Os resultados sugerem que um animal com doença policística felina pode ser tratado pela homeopatia.(AU)

The homeopathic treatment of a feline with polycystic kidney disease was evaluated, a common hereditary disease in the feline species. Because it is progressive, the prognosis depends on the stage of evolution of the chronic kidney disease, the feline response to the initial treatment and the guardian's desire to continue the treatment. The observation lasted 9 (nine) months and the evaluation of the results was performed through clinical examination and complementary tests such as ultrasound images and laboratory tests. The therapy was composed of constitutional Phosphorus 30CH and episodic Kresolum 6CH homeopathic medication associated with the introduction of diet kidney diet (adjunct dry feed). The homeopathic medicine did not cause adverse events in the animal. The results suggest that an animal with feline polycystic disease can be treated by homeopathy.(AU)

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OBJECTIVES: Autosomal dominant polycystic kidney disease (ADPKD), the most frequently diagnosed hereditary disease affecting Persian cats, is caused by a cytosine-to-adenine transversion (10063C>A) in PKD1, the gene that codes for polycystin-1. The objective of this study was to provide a preliminary estimate of the frequency of the pathogenic 10063C>A single nucleotide polymorphism (SNP) of PKD1 in Persian and Persian-related cat breeds in western Mexico. METHODS: Blood samples were collected from 104 cats (89 Persian, seven Persian crossbreed, five Siamese and three Himalayan cats). Genotyping was performed with our proposed PCR restriction fragment length polymorphism (RFLP) assay, as well as a previously established PCR-RFLP method for validation. The genotypes of control cats were corroborated by a commercial veterinary genetics laboratory. RESULTS: Our proposed PCR-RFLP assay and the validated PCR-RFLP methodology indicated that 24/104 (23.1%) cats in this study were heterozygous carriers of the 10063C>A SNP, including 23/89 Persian cats (25.8%) and 1/7 Persian crossbreed cats (14.3%). No Siamese or Himalayan cats were carriers. There were no discrepancies between the results obtained with our proposed assay and those obtained with the validation method or with commercial laboratory results. CONCLUSIONS AND RELEVANCE: The carrier frequency of the PKD1 10063C>A SNP in Persian and Persian-related cat breeds in western Mexico was found to be 23.1%. ADPKD frequencies among cat populations in Mexico have not been published previously. Genotyping assays can be used to facilitate the selection of breeding stocks by local breeders and veterinarians to avoid propagation of ADPKD.

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Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic disease in cats. However, scarce data on its prevalence are available in Brazil. Persian cats and Persian-related breeds were assessed by molecular genotyping for a C to A transversion in exon 29 of PKD1 gene to determine ADPKD prevalence in a Brazilian population. Genomic DNA extracted from peripheral whole blood or oral swabs samples was used to amplify exon 29 of PKD1 gene employing a PCR-RFLP methodology. From a total of 616 animals, 27/537 Persian and 1/17 Himalayan cats showed the single-nucleotide variant (C to A) at position 3284 in exon 29 of feline PKD1. This pathogenic variation has been identified only in heterozygous state. The prevalence of ADPKD in Persian cats and Persian-related breeds was 5.03% and 1.6%, respectively. There was no significant association between feline breed, gender or age with ADPKD prevalence. Of note, the observed ADPKD prevalence in Persian cats and Persian-related breeds in Brazil was lower than the ones reported in other parts of the world. This finding may be related to genetic counseling and consequent selection of ADPKD-free cats for reproduction.(AU)

A doença renal policística autossômica dominante (DRPAD) é a doença genética mais comum em gatos. No entanto, poucos dados sobre sua prevalência estão disponíveis no Brasil. Gatos Persas e de raças relacionadas foram avaliados por genotipagem molecular para a transversão CA no exon 29 do gene PKD1 felino para determinar a prevalência de DRPAD. DNA genômico extraído de sangue total periférico ou amostras de swabs orais foram utilizados para amplificar o exon 29 do gene PKD1 pela técnica de PCR-RFLP. De um total de 616 gatos, 27/537 Persas e 1/17 Himalaia mostraram a variante de nucleotídeo único (CA) na posição 3284 no exon 29 do gene PKD1. Esta variante patogênica foi identificada apenas em heterozigose. A prevalência de DRPAD em gatos Persas e raças relacionadas foram de 5,03% e 1,6%, respectivamente. Não houve associações significativas entre raça, gênero ou idade dos felinos e incidência de DRPAD. A prevalência de DRPAD em gatos Persas e raças relacionadas no Brasil foi menor do que em outras partes do mundo, o que pode estar relacionado ao aconselhamento genético e consequente seleção de gatos sem ADPKD para reprodução.(AU)

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Background: Renal cystic diseases (RCD) are characterized by cystic structures on renal parenchyma associated withobstructive lesions, membranous disruptions, and/or growth disturbances. The polycystic kidney disease (PKD) showsspecific pathological characteristics, related to mutations on PKD1 and/or PKD2 chromosome locus on humans. In Persiancats and bull terriers the condition is like the human “adult-onset” PKD, while in Perendale sheep the “childhood”-like isdescribed. In cetaceans, RCD are reported, however the characterization of PKD is scarcely described. This report aimsto describe two cases of PKD and one of RCD in stranded Steno bredanensis, and to discuss the disease associated factors.Cases: Four rough-toothed-dolphins were found stranded in the Paraná coast, southern Brazil between 2016 to 2018,through the Santos Basin Beach Monitoring Project (PMP-BS), one of the systematic monitoring programs required byBrazilian Institute of Environment and Renewable Natural Resources (IBAMA) for the environmental licensing processof oil production and transport by Petrobras in the presalt province. In three animals histological sampling was performed.One of them (animal 3) was found alive, presenting altered buoyancy with lateralization to the right and signs of pneumonia. The blood analysis showed anemia and leukocytosis. The animal showed poor clinical prognosis, and even withsupportive treatment, come to death four days after the rescue. Routine autopsies were performed on all animals. Animals1 and 2 presented macroscopically enlarged kidneys containing disseminated cystic...(AU)

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Background: Renal cystic diseases (RCD) are characterized by cystic structures on renal parenchyma associated withobstructive lesions, membranous disruptions, and/or growth disturbances. The polycystic kidney disease (PKD) showsspecific pathological characteristics, related to mutations on PKD1 and/or PKD2 chromosome locus on humans. In Persiancats and bull terriers the condition is like the human “adult-onset” PKD, while in Perendale sheep the “childhood”-like isdescribed. In cetaceans, RCD are reported, however the characterization of PKD is scarcely described. This report aimsto describe two cases of PKD and one of RCD in stranded Steno bredanensis, and to discuss the disease associated factors.Cases: Four rough-toothed-dolphins were found stranded in the Paraná coast, southern Brazil between 2016 to 2018,through the Santos Basin Beach Monitoring Project (PMP-BS), one of the systematic monitoring programs required byBrazilian Institute of Environment and Renewable Natural Resources (IBAMA) for the environmental licensing processof oil production and transport by Petrobras in the presalt province. In three animals histological sampling was performed.One of them (animal 3) was found alive, presenting altered buoyancy with lateralization to the right and signs of pneumonia. The blood analysis showed anemia and leukocytosis. The animal showed poor clinical prognosis, and even withsupportive treatment, come to death four days after the rescue. Routine autopsies were performed on all animals. Animals1 and 2 presented macroscopically enlarged kidneys containing disseminated cystic...

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The success of ex situ survival assurance populations as tools for amphibian conservation depends on the health and reproductive success of founder populations. Necropsy examination and histopathology of animals that die in assurance populations are useful for the identification of population-limiting disease problems and can help to direct applied research efforts in areas such as amphibian husbandry and nutrition. This study reviewed postmortem findings in 167 frogs from 13 species that died in a large Panamanian rescue and survival assurance population between 2006 and 2011. Common problems identified in long-term captive animals, especially in Atelopus species, were epithelial squamous metaplasia suggestive of vitamin A deficiency and a polycystic nephropathy resembling lesions seen in laboratory animals with electrolyte imbalances. Metabolic bone disease was a significant contributor to morbidity in captive-bred juvenile frogs of Gastrotheca cornuta, Hemiphractus fasciatus, and Hylomantis lemur. Findings common to multiple species included poor overall nutritional condition that was sometimes attributable to maladaptation to captive husbandry and epidermal hyperplasia and hyperkeratosis possibly reflecting environmental skin irritation. Infectious diseases and endoparasitism were most common in recently captured animals and included chytridiomycosis and Rhabdias sp. lungworms. Applied research efforts to improve sustainability of survival assurance populations should focus on elucidating optimal husbandry practices for diverse species, improving methods for nutritional supplementation of cultured insects and examination of the role of water composition in disease development.

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Este relato descreve um caso de doença renal policística em um bovino, macho, mestiço, com um ano de idade. Ao exame clínicoobservou-se estado nutricional ruim, mucosas pálidas, desidratação moderada (8% a 10%), úlceras na região ventral da língua,áreas multifocais de hipotricose recobertas por crostas por todo o corpo e decúbito esterno-lateral permanente. Na avaliação dohemograma observou-se principalmente anemia arregenerativa e leucocitose devido à neutrofilia com desvio à [confirmar] esquerda.Na necropsia, os rins estavam aumentados de volume, pálidos e com a superfície natural finamente irregular. Histologicamente, haviasubstituição quase completa da cortical renal por múltiplos e pequenos cistos, distensão dos espaços de Bowman, regeneraçãotubular, fibrose, edema e leve infiltrado inflamatório linfoplasmocítico intersticial.(AU)

This report describes a case of polycystic kidney disease in a male, mixed breed bovine aged one year. On clinical examinationrevealed a poor nutritional status, pallid mucous membranes, moderated dehydration (8 to 10%), ulcers on the ventral portion ofthe tongue, multifocal areas of hypotrichosis covered with scabs throughout the entire body and permanent sternolateral decubitus.The blood exam revealed aregenerative anemia and leukocytosis (neutrophilia) with deviation to the left. The necropsy revealedenlarged, pallid kidneys with a finely irregular natural surface. The histological analysis revealed the nearly complete replacementof the renal cortex by numerous small cysts, distension of the Bowman space, tubular regeneration, fibrosis, edema and mildinterstitial lymphoplasmacytic inflammatory infiltrate.(AU)

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Este relato descreve um caso de doença renal policística em um bovino, macho, mestiço, com um ano de idade. Ao exame clínicoobservou-se estado nutricional ruim, mucosas pálidas, desidratação moderada (8% a 10%), úlceras na região ventral da língua,áreas multifocais de hipotricose recobertas por crostas por todo o corpo e decúbito esterno-lateral permanente. Na avaliação dohemograma observou-se principalmente anemia arregenerativa e leucocitose devido à neutrofilia com desvio à [confirmar] esquerda.Na necropsia, os rins estavam aumentados de volume, pálidos e com a superfície natural finamente irregular. Histologicamente, haviasubstituição quase completa da cortical renal por múltiplos e pequenos cistos, distensão dos espaços de Bowman, regeneraçãotubular, fibrose, edema e leve infiltrado inflamatório linfoplasmocítico intersticial.

This report describes a case of polycystic kidney disease in a male, mixed breed bovine aged one year. On clinical examinationrevealed a poor nutritional status, pallid mucous membranes, moderated dehydration (8 to 10%), ulcers on the ventral portion ofthe tongue, multifocal areas of hypotrichosis covered with scabs throughout the entire body and permanent sternolateral decubitus.The blood exam revealed aregenerative anemia and leukocytosis (neutrophilia) with deviation to the left. The necropsy revealedenlarged, pallid kidneys with a finely irregular natural surface. The histological analysis revealed the nearly complete replacementof the renal cortex by numerous small cysts, distension of the Bowman space, tubular regeneration, fibrosis, edema and mildinterstitial lymphoplasmacytic inflammatory infiltrate.

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A doença renal policística é uma doença hereditária, de caráter autossômico dominante e que acomete comumente os rins de gatos persas ou mestiços dessa raça. Os sinais da doença ocorrem de forma tardia, entre três a dez anos de idade, quando geralmente o quadro de insuficiência renal começa a se instalar. Atualmente o exame ultrassonográfico dos rins é de extrema importância, por ser um método não-invasivo mais prático para diagnosticar a presença de cistos renais. A presente revisão de literatura tem por objetivo relatar que esta enfermidade que possui uma relativa gravidade a qual necessidade de diagnóstico precoce para possibilitar uma melhor qualidade de vida ao animal, uma vez que não há um tratamento específico para a doença.

Polycystic kidney disease is an inherited disorder, autosomal dominant and commonly affects the kidneys of Persian cats or crossbreeds. The signs of the disease occur so late, between three and ten years of age, usually when the renal failure begins to install. Currently, ultrasound of the kidneys is extremely important, because it is a noninvasive method more practical for diagnosing the presence of renal cysts. The present review aims to report that this disease which has relative seriousness which need for early diagnosis to enable a better quality of life of the animal, since there is no specific treatment for the disease

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During the last 21 years, 7 adult captive Brazilian agoutis (Dasyprocta leporina) from 4 different zoologic gardens were necropsied and histologically examined at the Leibniz Institute for Zoo and Wildlife Research, Berlin, Germany. All animals had polycystic kidney disease as the major pathologic change. Except in 1 case, no clinical signs were recognized prior to death. The animals had macroscopic bilateral alterations of the kidneys ranging from granulated surfaces to severe polycystic changes. Microscopic examination revealed multifocal to generalized, moderate to severe cystic dilatations of Bowman's capsules and renal tubules, moderate mesangial and capsular proliferation of the renal corpuscles, mild interstitial fibrosis, and mild to moderate interstitial lympho-plasmacytic infiltrations. Little information is known about the genetic relationships of these animals, but breeding practice indicates a high possibility of inbred agouti zoo populations in Germany. This is the first report on polycystic kidney disease in Brazilian agoutis with possible genetic background.

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