1. [Gardner syndrome: possibility of early detection of carriers by examination of the ocular fundus?].
- Author
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Brazzola P, Vignanelli M, Levy C, and Martinoli S
- Subjects
- Chromosome Disorders, Gardner Syndrome diagnosis, Humans, Pedigree, Risk Factors, Chromosome Aberrations genetics, Gardner Syndrome genetics, Genes, Dominant genetics, Genetic Carrier Screening, Ophthalmoscopy, Pigment Epithelium of Eye pathology
- Abstract
Through indirect ophthalmoscopic examination it was possible to analyse three families originated from the same Swiss alpine valley (Poschiavo) and carrying Gardner syndrome (SdG) to check if their members with SdG were presenting hypertrophic changes of the retinal epithelium which is supposed to be an early symptom of that syndrome. This lesion was found to be present only in two out of 11 patients (18%) with at least one symptom of SdG. Because of its lacking sensitivity, ophthalmoscopic examination is not able to substitute colonoscopy as a valid screening method to find out which members of a SdG-family are at risk to develop colonic poliposis and cancer.
- Published
- 1992