New approaches to the autosomal recessive polycystic kidney disease patient with dual kidney-liver complications.


Improved neonatal medical care and renal replacement technology have improved the long-term survival of patients with ARPKD. Ten-yr survival of those surviving the first year of life is reported to be 82% and is continuing to improve further. However, despite increases in overall survival and improved treatment of systemic hypertension and other… (More)
DOI: 10.1111/petr.12076


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