Congenital hypertrophy of the retinal pigment epithelium (CHRPE) and familial adenomatous polyposis (FAP)
Author:
Publisher
Wiley
Subject
Ophthalmology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0420.1996.tb00704.x/fullpdf
Reference24 articles.
1. Congenital hypertrophy of the retinal pigment epithelium as a marker for familial adenomatous polyposis;Berk;Dis Colum Rectum,1988
2. Hypertrophy of the retinal pigment epithelium associated with Gardners syndrome;Blair;Am J Ophthalmol,1980
3. Localization of the gene for familial adenomatous polyposis on chromosome 5;Bodmer;Nature,1987
4. The management of familial polyposis coly;Bussey;Roy Coll Med Current Med Lit- Gastroenterol,1985
5. Congenital hypertrophy of retinal pigment epithelium: a sign of familial adenomatous polyposis;Chapman;Br Med J,1989
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1. Congenital Hypertrophy of the Retinal Pigment Epithelium (CHRPE) as a Screening Marker for Familial Adenomatous Polyposis (FAP): Systematic Literature Review and Screening Recommendations;Clinical Ophthalmology;2022-03
2. Torpedo-like lesions in the ocular fundi of Gardner syndrome: hiding in plain view;Ophthalmic Genetics;2021-05-20
3. Diffuse bear-track retina: profound, bilateral, grouped congenital pigmentation of the retinal pigment epithelium in an infant;Journal of American Association for Pediatric Ophthalmology and Strabismus;2020-12
4. In patients with a positive family history of familial adenomatous polyposis can the condition be diagnosed from the presence of congenital hypertrophy of the retinal pigment epithelium detected via an eye examination: A systematic review;Clinical & Experimental Ophthalmology;2019-10-10
5. Hereditary Cancer Syndromes—A Primer on Diagnosis and Management, Part 2: Gastrointestinal Cancer Syndromes;Mayo Clinic Proceedings;2019-06
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