A complex case of congenital cystic renal disease

Autor:	Maeve McPhillips, David S Cordiner, Marie-Anne Brundler, Mark Darling, Enric Murio, Sepideh Taheri, Clair Evans
Rok vydání:	2012
Předmět:	Diagnostic Imaging Pathology medicine.medical_specialty Biopsy medicine.medical_treatment Disease Nephrectomy Article Diagnosis Differential Humans Medicine Intensive care medicine Kidney transplantation Polycystic Kidney Autosomal Recessive business.industry Infant Newborn Renal medicine General Medicine medicine.disease Combined Modality Therapy Kidney Transplantation Autosomal Recessive Polycystic Kidney Disease Liver Transplantation Chronic renal failure Female Differential diagnosis business Immunosuppressive Agents Rare disease
Zdroj:	Case Reports. 2012:bcr1220115463-bcr1220115463
ISSN:	1757-790X
DOI:	10.1136/bcr.12.2011.5463
Popis:	This case outlines the potential complexity of autosomal recessive polycystic kidney disease (ARPKD). It highlights the challenges involved in managing this condition, some of the complications faced and areas of uncertainty in the decision making process. With a paucity of published paediatric cases on this subject, this should add to the pool of information currently available.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c77d8517993fe959a7c1fddfcebf8c34 https://doi.org/10.1136/bcr.12.2011.5463 Zobrazit plný text záznamu