Two Cases of Congenital Hypertrophy of Retinal Pigment Epithelium Associated with Familial Adenomatous Polyposis
Journal of the Korean Ophthalmological Society
;
: 662-666, 1992.
Article
in Korean
| WPRIM
| ID: wpr-10284
ABSTRACT
Familial adenomatous polyposis (FAP) is a rare hereditary disease that undergo malignant change and recent reports have described a very high incidence (87.5%-100.0%) of congenital hypertrophy of the retinal pigment epithelium (CHRPE) in Gardner's syndrome and familial adenomatous polyposis. Recognization of CHRPE lesion in ophthalmological screening test for the familial members with FAP is helpful not only in prediciting the presence of adenomatous polyposis and malignant carcinoma but also in genetic counselling. Authors have examined and report 2 female patients with similar CHRPE lesions in both fundus and thus diagnosed FAP following surgical examination.
Full text:
Available
Index:
WPRIM (Western Pacific)
Main subject:
Retinaldehyde
/
Gardner Syndrome
/
Mass Screening
/
Incidence
/
Adenomatous Polyposis Coli
/
Retinal Pigment Epithelium
/
Genetic Diseases, Inborn
/
Hypertrophy
Type of study:
Incidence study
/
Prognostic study
/
Screening study
Limits:
Female
/
Humans
Language:
Korean
Journal:
Journal of the Korean Ophthalmological Society
Year:
1992
Type:
Article
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