Disorders of optic nerve and visual pathways
Description
Foster-Kennedy syndrome: Conditions which produce injury or dysfunction of the second cranial or optic nerve, which is generally considered a component of the central nervous system. Damage to optic nerve fibers may occur at or near their origin in the retina, at the optic disk, or in the nerve, optic chiasm, optic tract, or lateral geniculate nuclei. Clinical manifestations may include decreased visual acuity and contrast sensitivity, impaired color vision, and an afferent pupillary defect.
Data source
FinnGen phenocode | H7_OPTNERVE |
Hospital Discharge registry | ICD-10: H46/H47 |
Cause of Death registry | ICD-10: H46/H47 |
Include | H7_OPTNEURITIS, H7_OPTNEUROTH, H7_RETROBULBNEURINOTH, H7_OPTNERVPATHINOTH |
Level in the ICD-hierarchy | 2 |
First defined in version | DF2 |
Key figures
Sex | All | Female | Male |
Number of individuals | 726 | 466 | 260 |
Unadjusted prevalence (%) | 0.55 | 0.62 | 0.45 |
Mean age at first event (years) | 46.27 | 43.96 | 50.41 |
Median number of events / individual | 2 | 2 | 1 |
Clinical metrics
Sex | All | Female | Male |
Recurrence within 6 months (%) | 39.53 | 40.56 | 37.69 |
Case fatality at 5-years (%) | 3.17 | 2.58 | 4.23 |