Dominant optic atrophy
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Dominant optic atrophy. / Lenaers, Guy; Hamel, Christian; Delettre, Cécile; Amati-Bonneau, Patrizia; Procaccio, Vincent; Bonneau, Dominique; Reynier, Pascal; Milea, Dan.
In: Orphanet Journal of Rare Diseases, Vol. 7, 2012, p. 46.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Dominant optic atrophy
AU - Lenaers, Guy
AU - Hamel, Christian
AU - Delettre, Cécile
AU - Amati-Bonneau, Patrizia
AU - Procaccio, Vincent
AU - Bonneau, Dominique
AU - Reynier, Pascal
AU - Milea, Dan
PY - 2012
Y1 - 2012
N2 - DEFINITION OF THE DISEASE: Dominant Optic Atrophy (DOA) is a neuro-ophthalmic condition characterized by a bilateral degeneration of the optic nerves, causing insidious visual loss, typically starting during the first decade of life. The disease affects primary the retinal ganglion cells (RGC) and their axons forming the optic nerve, which transfer the visual information from the photoreceptors to the lateral geniculus in the brain.
AB - DEFINITION OF THE DISEASE: Dominant Optic Atrophy (DOA) is a neuro-ophthalmic condition characterized by a bilateral degeneration of the optic nerves, causing insidious visual loss, typically starting during the first decade of life. The disease affects primary the retinal ganglion cells (RGC) and their axons forming the optic nerve, which transfer the visual information from the photoreceptors to the lateral geniculus in the brain.
U2 - 10.1186/1750-1172-7-46
DO - 10.1186/1750-1172-7-46
M3 - Journal article
C2 - 22776096
VL - 7
SP - 46
JO - Orphanet Journal of Rare Diseases
JF - Orphanet Journal of Rare Diseases
SN - 1750-1172
ER -
ID: 48527053