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TitleRelative frequencies of congenital colour vision deficiencies seen at the Ghent University Hospital
Abstract Nr.P016
PurposeAs a group, congenital colour vision (CV) deficiencies are rather frequent. Traditionally they include trichromatic deuteranomaly (DA), protanomaly (PA) and the dichromatic deuteranopia (D) and protanopia (P). Tritanomaly (TA) and tritanopia (T), blue cone monochromacy (BCM) and complete achromatopsia (CA) are all less frequent. Here, results of CV screening of such patients seen during 49 years at the Ghent University Hospital (GUH) are presented.
MethodsA total of 3289 patients (>99% males) referred because of problems with CV were examined from 1955 until 2004. To evaluate a potential referral bias prior to a change in the Belgian law (RD of 23/03/1998) allowing patients with P to drive from then onwards, patients examined after the introduction of that law were also analysed as a separate subgroup. All patients were examined using standard CV tests under C-light, including PIC-plates, ranking tests & anomaloscopy.
ResultsThe breakdown of the 3289 patients in decreasing order is as follows: 42% DA, 20% P, 19% D, 13% PA, and <1% CA, unknowns, BCM, TA, and 4% normals.
The figures for 215 patients seen after introduction of the RD of 23/03/1998 are: 35% DA, 22% P, 20% PA, 14% D, 1% CA & 7% normals.
ConclusionRelative frequencies of congenital CV deficiencies in patients seen at the GUH show a relative underrepresentation of DA and an overrepresentation of P & D. This is true when evaluating both total numbers and the numbers after a change in Belgian law allowing P patients to drive. Consequently, the relatively mild character of DA may be a more important referral bias.
Author 1
Last nameUVIJLS
InitialsA
DepartmentGhent Univ Hospital
CityGhent
Author 2
Last nameDE BIE
InitialsS
DepartmentGhent Univ Hospital
CityGhent
Author 3
Last nameKESTELYN
InitialsP
DepartmentGhent Univ Hospital
CityGhent
Author 4
Last nameLEROY
InitialsBP
DepartmentGhent Univ Hospital
CityGhent
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