Your browser doesn't support javascript.
loading
Montrer: 20 | 50 | 100
Résultats 1 - 1 de 1
Filtre
Ajouter des filtres








Gamme d'année
1.
Journal of the Korean Neurological Association ; : 95-98, 1998.
Article Dans Coréen | WPRIM | ID: wpr-161943

Résumé

Leber's Hereditary Optic Neuropathy(LHON) is a maternally inherited disorders that occurs primarily in young males and is characterized by subacute, sequential, bilateral central visual loss, ultimately, optic atrophy. We report 2 cases of molecularly confirmed LHON which reveal 11778 and 14484 mitochondral DNA mutation, respectively but there is no family history of visual loss. So the diagnosis of LHON deserves to be considered in all crypotogenic cases of acute or subacute optic or chiasmal neuropathy. Late or early age at onset, female gender, and a negative family history should not be dissuasive.


Sujets)
Femelle , Humains , Mâle , Diagnostic , ADN , Biologie moléculaire , Atrophie optique , Atteintes du nerf optique
SÉLECTION CITATIONS
Détails de la recherche