Literature DB >> 11405352

Diagnosis of mitochondrial disorders: clinical and biochemical approach.

D R Thorburn1, J Smeitink.   

Abstract

The topic of Workshop W3-1 was clinical and biochemical approaches to the diagnosis of mitochondrial respiratory chain disorders. Four main questions were addressed in an attempt to make some progress towards a consensus diagnostic approach: What are the major limitations in diagnosis of respiratory chain dysfunction? What is the ideal approach to investigating children with a suspected respiratory chain disorder? Can we begin to develop consensus diagnostic criteria? Can we develop a quality assurance (QA) scheme for respiratory chain enzyme assays? The workshop demonstrated strong consensus on recognizing the limitations of current diagnostic approaches, on the ideal diagnostic approach and on the desirability of an enzyme QA scheme. There was also support for the desirability of consensus diagnostic criteria, albeit with some concerns about the practicality of gaining consensus. Two potential approaches to developing consensus criteria were described.

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Year:  2001        PMID: 11405352     DOI: 10.1023/a:1010347808082

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  18 in total

1.  Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.

Authors:  Sarah E Calvo; Alison G Compton; Steven G Hershman; Sze Chern Lim; Daniel S Lieber; Elena J Tucker; Adrienne Laskowski; Caterina Garone; Shangtao Liu; David B Jaffe; John Christodoulou; Janice M Fletcher; Damien L Bruno; Jack Goldblatt; Salvatore Dimauro; David R Thorburn; Vamsi K Mootha
Journal:  Sci Transl Med       Date:  2012-01-25       Impact factor: 17.956

2.  Neuroradiologic findings in children with mitochondrial disorder: correlation with mitochondrial respiratory chain defects.

Authors:  Jinna Kim; Seung-Koo Lee; Eung Yeop Kim; Dong Ik Kim; Young-Mock Lee; Joon Soo Lee; Heung Dong Kim
Journal:  Eur Radiol       Date:  2008-04-04       Impact factor: 5.315

Review 3.  Biochemical diagnosis of mitochondrial disorders.

Authors:  Richard J T Rodenburg
Journal:  J Inherit Metab Dis       Date:  2010-05-04       Impact factor: 4.982

Review 4.  Mitochondrial disorders: prevalence, myths and advances.

Authors:  D R Thorburn
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

Review 5.  Mitochondrial disorders: clinical presentation and diagnostic dilemmas.

Authors:  J A M Smeitink
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

Review 6.  Anesthesia for children with mitochondrial disorders: a national survey and review.

Authors:  Muhammad B Rafique; Staci D Cameron; Qaiser Khan; Suur Biliciler; Salman Zubair
Journal:  J Anesth       Date:  2012-09-25       Impact factor: 2.078

7.  Inherited disorders affecting mitochondrial function are associated with glutathione deficiency and hypocitrullinemia.

Authors:  Kondala R Atkuri; Tina M Cowan; Tony Kwan; Angelina Ng; Leonard A Herzenberg; Leonore A Herzenberg; Gregory M Enns
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-17       Impact factor: 11.205

Review 8.  Presentation and diagnosis of mitochondrial disorders in children.

Authors:  Mary Kay Koenig
Journal:  Pediatr Neurol       Date:  2008-05       Impact factor: 3.372

Review 9.  Prerequisites and strategies for prenatal diagnosis of respiratory chain deficiency in chorionic villi.

Authors:  L Niers; L van den Heuvel; F Trijbels; R Sengers; J Smeitink
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

10.  Next generation sequence analysis for mitochondrial disorders.

Authors:  Valeria Vasta; Sarah B Ng; Emily H Turner; Jay Shendure; Si Houn Hahn
Journal:  Genome Med       Date:  2009-10-23       Impact factor: 11.117

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