Literature DB >> 9677732

Kearns-Sayre syndrome. A case report.

S Altunbaşak1, G Bingöl, N Ozbarlas, Z Akçören, O Hergüner.   

Abstract

Kearns-Sayre syndrome (KSS) is a mitochondrial disorder. There is a large-scale mitochondrial DNA (mtDNA) deletion in most of the case. In this article, a case of KSS who has progressive external ophthalmoplegia (PEO), retinitis pigmentosa (RP), complete heart block, encephalopathy attacks, type-1 diabetes mellitus, ragged-red fiber (RRF) and lactic acidosis is presented and discussed in light of the literature available on this subjects. Diagnosis is confirmed by determination of mtDNA deletion.

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Year:  1998        PMID: 9677732

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  1 in total

1.  Hypoparathyroidism as the first manifestation of kearns-sayre syndrome: a case report.

Authors:  Farah Ashrafzadeh; Nosrat Ghaemi; Javad Akhondian; Mehran Beiraghi Toosi; Saghi Elmi
Journal:  Iran J Child Neurol       Date:  2013
  1 in total

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