Mitochondrial tubulopathy : the many faces of mitochondrial disorders

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 mitochondri...

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Veröffentlicht in:Pediatric nephrology (Berlin, West) West), 2001-09, Vol.16 (9), p.710-712
Hauptverfasser: YUNG SENG LEE, HUI KIM YAP, BARSHOP, Bruce A, YOKE SUN LEE, RAJALINGAM, Sinniah, KAH YIN LOKE
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Sprache:eng
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Zusammenfassung: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.
ISSN:0931-041X
1432-198X
DOI:10.1007/s004670100637