Caso clínico
Neuropatía óptica hereditaria de Leber por mutación G11778A del ADN mitocondrial. Manejo de un caso
Leber's hereditary optic neuropathy with G11778A mutation in mitochondrial DNA. Management of a case
David Barreda Gagoa,
, Isabel Gómez Ledesmab, María de los Ángeles Santiago Rodríguezc, Emiliano Hernández Galilead
Autor para correspondencia
a Médico interno residente de Oftalmología de 4.o año, Complejo Asistencial Hospitalario de Salamanca, Sanidad de Castilla y León (SACYL), Salamanca, España
b Facultativo especialista en Oftalmología, Complejo Asistencial Hospitalario de Salamanca, Sanidad de Castilla y León (SACYL), Salamanca, España
c Facultativo especialista en Oftalmología, Jefa de Sección, Complejo Asistencial Hospitalario de Salamanca, Sanidad de Castilla y León (SACYL), Salamanca, España
d Facultativo especialista en Oftalmología, Jefe del Servicio de Oftalmología, Complejo Asistencial Hospitalario de Salamanca, Sanidad de Castilla y León (SACYL), Salamanca, España
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