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The Phenotypic Spectrum of 47 Czech Patients with Single, Large-Scale Mitochondrial DNA Deletions.

Nicole AnteneováSilvie KelifováHana KolářováAlžběta VondráčkováIveta TóthováPetra LiškováMartin MagnerJosef ZámečníkHana HansíkováJiří ZemanMarkéta TesařováTomáš Honzík
Published in: Brain sciences (2020)
Paediatric manifestation of Progressive External Ophthalmoplegia (PEO) is not associated with a higher risk of multisystemic involvement. Contrary to PEO and Kearns-Sayre Syndrome Spectrum, Pearson Syndrome still contributes to a significant childhood mortality. SLSMD should be considered even in cases with atypical presentation. To successfully identify carriers of SLSMD, a repeated combined analysis of buccal swab and urinary epithelial cells is needed.
Keyphrases
  • mitochondrial dna
  • copy number
  • case report
  • multiple sclerosis
  • emergency department
  • intensive care unit
  • cardiovascular events
  • risk factors
  • type diabetes
  • cardiovascular disease
  • genome wide
  • young adults