Four pediatric patients with autosomal recessive polycystic kidney disease developed new‐onset diabetes after renal transplantation | Zendy

Carter S. A. | Zendy; Kitching A. R. | Zendy; Johnstone L. M. | Zendy

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Four pediatric patients with autosomal recessive polycystic kidney disease developed new‐onset diabetes after renal transplantation

Author(s) -

Carter S. A.,

Kitching A. R.,

Johnstone L. M.

Publication year - 2014

Publication title -

pediatric transplantation

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.457

H-Index - 69

eISSN - 1399-3046

pISSN - 1397-3142

DOI - 10.1111/petr.12332

Subject(s) - medicine , transplantation , pediatrics , polycystic kidney disease , diabetes mellitus , renal transplant , autosomal recessive polycystic kidney disease , disease , risk factor , kidney transplantation , intensive care medicine , endocrinology

NODAT is increasingly prevalent. Compared with adult recipients, NODAT is less prevalent in pediatric renal transplant recipients; however, some risk factors for its development in young patients have been defined. We report four pediatric renal transplant recipients with ARPKD who developed NODAT . We review the current pediatric NODAT literature and hypothesize that ARPKD may be an additional risk factor for NODAT .

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