Diagnostic implications of Gardner Syndrome, case report of a familial adenomatous polyposis (FAP) variant, for eye care professionals
International Journal of Surgery Case Reports, ISSN: 2210-2612, Vol: 116, Page: 109379
2024
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
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Case Description
Gardner Syndrome (GS) is a variant of Familial Adenomatous Polyposis (FAP). FAP is characterized by several precancerous adenomatous intestinal polyps while GS has additional distinct extraintestinal features such as congenital hypertrophy of retinal epithelium (CHRPE), which we describe here. 42-year-old male with GS presenting with flashes and floaters observed to have CHRPE-like lesions characteristic of GS. Subtle CHRPE findings differentiate pathological, described in the present case, from non-pathological etiologies and may guide further management. Here we present the signs and symptoms that raise suspicion for GS associated with CHRPE and how to approach management late in the disease presentation.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S2210261224001603; http://dx.doi.org/10.1016/j.ijscr.2024.109379; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85184831963&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/38350372; https://linkinghub.elsevier.com/retrieve/pii/S2210261224001603; https://dx.doi.org/10.1016/j.ijscr.2024.109379
Elsevier BV
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