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Kearns-Sayre syndrome in twins: lethal dominant mutation or acquired disease?
Rowland, L P; Hausmanowa-Petrusewicz, I; Bardurska, B; Warburton, D; Nibroj-Dobosz, I; DiMauro, S; Pallai, M; Johnson, W G.
Afiliación
  • Rowland LP; Neurological Institute, Columbia-Presbyterian Medical Center, New York, NY 10032-3784.
Neurology ; 38(9): 1399-402, 1988 Sep.
Article en En | MEDLINE | ID: mdl-3412586
ABSTRACT
We studied twin brothers who met all diagnostic criteria for the Kearns-Sayre syndrome (KSS). The twins reinforce the view that KSS is a specific syndrome. They raise the possibility that the condition is inherited as a lethal dominant trait, a mode of inheritance that explains the observed paucity of familial cases. However, these cases do not exclude the possibility of an acquired cause, such as persistent viral infection of the brain.
Asunto(s)
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oftalmoplejía / Síndrome de Kearns-Sayre / Enfermedades en Gemelos Tipo de estudio: Etiology_studies Límite: Adult / Humans / Male Idioma: En Revista: Neurology Año: 1988 Tipo del documento: Article
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oftalmoplejía / Síndrome de Kearns-Sayre / Enfermedades en Gemelos Tipo de estudio: Etiology_studies Límite: Adult / Humans / Male Idioma: En Revista: Neurology Año: 1988 Tipo del documento: Article