Literature DB >> 9168163

A PCR test for progressive external ophthalmoplegia and Kearns-Sayre syndrome on DNA from blood samples.

I F De Coo1, T Gussinklo, P J Arts, B A Van Oost, H J Smeets.   

Abstract

Progressive external ophthalmoplegia (PEO) and Kearns-Sayre syndrome (KSS) are caused by deletions in mitochondrial DNA. Identification of these deletions is important for diagnosis, prognosis and genetic counselling. As yet, the most frequently used test is Southern blot analysis of DNA isolated from a muscle biopsy. Here, we describe a sensitive PCR-based test for the identification of these deletions in DNA isolated from blood. The main advantage is that in the majority of cases a muscle biopsy is no longer necessary for the molecular diagnosis of PEO and KSS.

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Year:  1997        PMID: 9168163     DOI: 10.1016/s0022-510x(97)05366-5

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  2 in total

1.  A rare case report of simultaneous presentation of myopathy, Addison's disease, primary hypoparathyroidism, and Fanconi syndrome in a child diagnosed with Kearns-Sayre syndrome.

Authors:  Meropi Tzoufi; Alexandros Makis; Nikolaos Chaliasos; Iliada Nakou; Ekaterini Siomou; Agathoklis Tsatsoulis; Anastasia Zikou; Maria Argyropoulou; Jean Paul Bonnefont; Antigone Siamopoulou
Journal:  Eur J Pediatr       Date:  2012-08-09       Impact factor: 3.183

2.  Progressive External Ophthalmoplegia Diagnosed in the Glaucoma Clinic: The Importance of a Complete Clinical Examination.

Authors:  Dimitrios Karagiannis; Loukas Kontomichos; Vasileios Tzimis; Efstratios Parikakis; Georgios Batsos; Michael Karampelas
Journal:  Clin Optom (Auckl)       Date:  2021-12-24
  2 in total

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