Wolff-Parkinson-White syndrome and noncompaction in Leber’s hereditary optic neuropathy due to the variant m.3460G>A

This report describes a 66-year-old Caucasian male who acutely developed severe, bilateral impairment of visual acuity at 24 years of age. Leber’s hereditary optic neuropathy (LHON) was suspected but the diagnosis was not genetically confirmed until the age of 49 years when the primary LHON mutation...

Descripción completa

Detalles Bibliográficos
Autores principales: Finsterer, Josef, Stollberger, Claudia, Gatterer, Edmund
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991228/
https://www.ncbi.nlm.nih.gov/pubmed/29562793
http://dx.doi.org/10.1177/0300060518765846

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991228/
https://www.ncbi.nlm.nih.gov/pubmed/29562793
http://dx.doi.org/10.1177/0300060518765846

Ejemplares similares