Acute Tubular Dysfunction With Fanconi Syndrome: A New Manifestation of Mitochondrial Cytopathies

Received 8 June 2007; accepted 13 November 2007.

Index Words: Mitochondria, tubulopathy, Fanconi syndrome, metabolism, inborn error, acidosis, episodic

No abstract is available. To read the body of this article, please view the Full Text online.

1 Division of Medical Genetics, Department of Pediatrics, Montreal Children Hospital, McGill University, Montreal, Québec, Canada

2 Division of Nephrology, Department of Pediatrics, Montreal Children Hospital, McGill University, Montreal, Québec, Canada

3 Department of Pathology, CHU Sainte-Justine, Montreal Children Hospital, McGill University, Montreal, Québec, Canada

4 Department of Pathology, Montreal Children Hospital, McGill University, Montreal, Québec, Canada

5 Metabolism Research Program, Research Institute, Department of Pediatrics and Biochemistry, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.

Address correspondence to Grant A. Mitchell, MD, CHU Sainte-Justine, 3175 Côte Sainte-Catherine, Montréal, Québec, H3T 1C5, Canada.

PII: S0272-6386(07)01610-1

doi:10.1053/j.ajkd.2007.11.024

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