Article
Atypical glomerulopathy associated with the cblE inborn error of vitamin B₁₂ metabolism.
Pediatric nephrology (Berlin, Germany) - 1 Jul 2013
Paul Erin A, Guttenberg Marta, Kaplan Paige, Watkins David, Rosenblatt David S, Treat James R, Kaplan Bernard S
Abstract excerpt
BACKGROUND: The cblE disorder is an inherited disorder of vitamin B12 metabolism that results in elevated levels of homocysteine and decreased methionine in body fluids. Renal complications have been reported in patients with cblC disease, but not in those with cblE disease. The renal complications of cblC disease include thrombotic microangiopathy (TMA), neonatal hemolytic uremic syndrome, chronic renal failure,...
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