Article
Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with pearson syndrome.
American journal of human genetics - 1 Sept 2002
Shanske Sara, Tang Yingying, Hirano Michio, Nishigaki Yutaka, Tanji Kurenai, Bonilla Eduardo, Sue Carolyn, Krishna Sindu, Carlo Jose R, Willner Judith, Schon Eric A, DiMauro Salvatore
Abstract excerpt
Single deletions of mitochondrial DNA (mtDNA) are associated with three major clinical conditions: Kearns-Sayre syndrome, a multisystem disorder; Pearson syndrome (PS), a disorder of the hematopoietic system; and progressive external ophthalmoplegia (PEO), primarily affecting the ocular muscles. Typically, single mtDNA deletions are sporadic events, since the mothers, siblings, and offspring of affected...
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