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Mitochondrial tubulopathy: the many faces of mitochondrial disorders
Y S Lee1, H K Yap, B A Barshop
1Department of Pediatrics, National University of Singapore, Singapore. paeleeys@nus.edu.sg
Pediatric Nephrology (Berlin, Germany)
|August 21, 2001
Abstract:
We report a rare presentation of mitochondrial disorder in a child with recurrent carpopedal spasms due to hypocalcemia and hypomagnesemia, secondary to renal proximal tubulopathy and possible hypoparathyroidism. At least two mutant mitochondrial DNA species were identified, and abnormal mitochondria were found in the muscle and renal biopsy specimens. The case illustrates the spectrum and diversity of mitochondrial presentations, arising because of heteroplasmy of mutations and the type of organs affected.