Two Cases of Leber's Hereditary Optic Atrophy Occurred in Mother and Son
Journal of the Korean Ophthalmological Society
;
: 867-871, 1982.
Article
in Korean
| WPRIM
| ID: wpr-104037
ABSTRACT
Leber's hereditary optic atrophy is characterized by sudden loss of central vision occuringin the second and third decade of life and nondirect transmission with male preponderance, Leber disease affecting both eyes in different degree and not simultaneouly, showing in its. early stage hyperemia of optic disc followes by a secondary atrophy, which involves a serious permanent impairment of central vision. Recently, the auther have been experienced Leber hereditary optic atrophy in 30 years old mother and 12 years old son, with severe impaiarment of visual acuity and central scotoma in both eyes and had pallor on the discs. Clinical ophthalmoscopic, perimetric, color vision test and neurologic examination were performed in two persons.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Pallor
/
Atrophy
/
Scotoma
/
Visual Acuity
/
Optic Atrophy, Hereditary, Leber
/
Color Vision
/
Hyperemia
/
Mothers
/
Neurologic Examination
Limits:
Adult
/
Child
/
Humans
/
Male
Language:
Korean
Journal:
Journal of the Korean Ophthalmological Society
Year:
1982
Type:
Article
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