Literature DB >> 10913735

Mitochondrial cytopathy combined with Fanconi's syndrome.

L C Wang1, W T Lee, W Y Tsai, Y K Tsau, Y Z Shen.   

Abstract

Severe muscle weakness in Fanconi's syndrome is rarely the result of mitochondrial cytopathy. We describe a rare case of a 9-year-old male with early onset of Fanconi's syndrome. He developed severe proximal muscle weakness exacerbated by hypokalemia and hypophosphatemia in childhood. The muscle biopsy revealed increased accumulation of abnormal mitochondria and fat droplets in histochemical stains and electron microscopy. Mitochondrial cytopathy cannot be excluded in Fanconi's syndrome with late onset of muscular impairment. Long-term follow-up of his clinical course is suggested to understand the natural history of this unusual case.

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Year:  2000        PMID: 10913735     DOI: 10.1016/s0887-8994(00)00128-4

Source DB:  PubMed          Journal:  Pediatr Neurol        ISSN: 0887-8994            Impact factor:   3.372


  1 in total

1.  A mitochondrial DNA deletion presenting with corneal clouding and severe Fanconi syndrome.

Authors:  Joyce J Lee; Laura M Tripi; Richard W Erbe; Sudha Garimella-Krovi; James E Springate
Journal:  Pediatr Nephrol       Date:  2012-01-20       Impact factor: 3.714

  1 in total

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