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10.3389/fped.2017.00124 http://scihub22266oqcxt.onion/10.3389/fped.2017.00124 C5446979!5446979 !28611971     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28611971 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       Front+Pediatr 2017 ; 5 (?): 124 Nephropedia Template TP {{tp|p=28611971 |t=2017. Diagnosis and Management of Hepatobiliary Complications in Autosomal Recessive Polycystic Kidney Disease |pdf=|usr=}}{{28611971 }} gab.com Text Diagnosis and Management of Hepatobiliary Complications in Autosomal Recessive Polycystic Kidney Disease JO: Front Pediatr http://www.kidney.de/pget.php?&tw=1&pmid=28611971 #FOAvip Autosomal recessive polycystic kidney disease (ARPKD) is a congenital hepatorenal fibrocystic disease. The hepatic manifestations of ARPKD can range from asymptomatic to portal hypertension and massively dilated biliary system that results in liver transplantation. Hepatic complications of ARPKD typically present with signs of portal hypertension (splenomegaly and thrombocytopenia) or cholangitis. Liver disease in ARPKD does not always correlate with severity of renal disease. Management of ARPKD-related liver disease is largely treating specific symptoms, such as antibiotics for cholangitis or endoscopic treatment for variceal bleeding. If complications cannot be managed medically, liver transplantation may be indicated. This mini-review will discuss the clinical manifestations and management of children with ARPKD liver disease. Twit Text FOAVip Diagnosis and Management of Hepatobiliary Complications in Autosomal Recessive Polycystic Kidney Disease ????Front Pediatr http://www.kidney.de/pget.php?&tw=1&pmid=28611971 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28611971 #FOAvip English Wikipedia <ref>{{Cite pmid|28611971 }}</ref> Diagnosis and Management of Hepatobiliary Complications in Autosomal Recessive Polycystic Kidney Disease #MMPMID28611971 Wehrman A ; Kriegermeier A ; Wen J Front Pediatr 2017[]; 5 (?): 124 PMID28611971 show ga Autosomal recessive polycystic kidney disease (ARPKD) is a congenital hepatorenal fibrocystic disease. The hepatic manifestations of ARPKD can range from asymptomatic to portal hypertension and massively dilated biliary system that results in liver transplantation. Hepatic complications of ARPKD typically present with signs of portal hypertension (splenomegaly and thrombocytopenia) or cholangitis. Liver disease in ARPKD does not always correlate with severity of renal disease. Management of ARPKD-related liver disease is largely treating specific symptoms, such as antibiotics for cholangitis or endoscopic treatment for variceal bleeding. If complications cannot be managed medically, liver transplantation may be indicated. This mini-review will discuss the clinical manifestations and management of children with ARPKD liver disease. ?Diagnosis and Management of Hepatobiliary Complications in Autosomal R(epmc).pdf DeepDyve Pubget Overpricing