Novel TK2 mutations as a cause of delayed muscle maturation in mtDNA depletion syndrome

نویسندگان

  • Thanes Termglinchan
  • Seito Hisamatsu
  • Junko Ohmori
  • Hiroshi Suzumura
  • Noriko Sumitomo
  • George Imataka
  • Osamu Arisaka
  • Nobuyuki Murakami
  • Narihiro Minami
  • Ishiyama Akihiko
  • Masayuki Sasaki
  • Yuichi Goto
  • Satoru Noguchi
  • Ikuya Nonaka
  • Satomi Mitsuhashi
  • Ichizo Nishino
چکیده

Recessive mutations in TK2 cause a severe mitochondrial DNA depletion syndrome (MDS),(1) characterized by severe myopathy from early infancy. Recent reports have suggested a wider clinical spectrum including encephalomyopathic form.(1,2) We report a patient with infantile-onset fatal encephalomyopathy presenting with extreme muscle fiber immaturity.

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Thymidine kinase 2 defects can cause multi-tissue mtDNA depletion syndrome.

Mitochondrial DNA depletion syndrome (MDS) is a severe recessively inherited disease of childhood. It manifests most often in infancy, is rapidly progressive and leads to early death. MDS is caused by an increasing number of nuclear genes leading to multisystemic or tissue-specific decrease in mitochondrial DNA (mtDNA) copy number. Thymidine kinase 2 (TK2) has been reported to cause a myopathic...

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عنوان ژورنال:

دوره 2  شماره 

صفحات  -

تاریخ انتشار 2016