| Literature DB >> 16217264 |
Antonino Trizzino1, Piero Farruggia, Delia Russo, Paolo D'Angelo, Serena Tropia, Vincenzo Benigno, Giuseppe Tarantino, Vito Di Marco, Maurizio Aricò.
Abstract
The disease presentation of autosomal recessive polycystic kidney disease (OMIM #263200, ARPKD) is highly variable and includes polycystic kidneys, pulmonary hypoplasia, and congenital hepatic fibrosis. The authors report an unusual case of ARPKD presenting with hepatosplenomegaly and cytopenia mimicking acute leukemia.Entities:
Mesh：
Year: 2005 PMID： 16217264 DOI： 10.1097/01.mph.0000184577.46458.7e
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN： 1077-4114 Impact factor: 1.289