Congenital hepatic fibrosis and polycystic kidney disease not linked to C >A mutation in exon 29 of PKD1 in a Persian cat

CASE SUMMARY: We describe the case of a 1-year-old male Persian cat diagnosed with congenital hepatic fibrosis (CHF) associated with renal polycystic disease and, for the first time, we have shown that there was no C >A mutation in exon 29 of PKD1 (polycystic kidney disease 1). The cat presented...

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Detalles Bibliográficos
Autores principales: Guerra, Juliana Mariotti, Daniel, Alexandre Gonçalves Teixeira, Cardoso, Natalia Cavalca, Grandi, Fabrizio, Queiroga, Felisbina, Cogliati, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362006/
https://www.ncbi.nlm.nih.gov/pubmed/28491400
http://dx.doi.org/10.1177/2055116915619191

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5362006/
https://www.ncbi.nlm.nih.gov/pubmed/28491400
http://dx.doi.org/10.1177/2055116915619191

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