AI Article Synopsis

  • A rare case of preretinal granules was found in an 18-year-old male with atypical familial exudative vitreoretinopathy (FEVR), which had been observed since he was five years old.
  • The patient underwent genetic testing, but results showed no known pathogenic variants associated with FEVR, suggesting an unusual cause for his symptoms.
  • A literature review identified five similar cases, indicating that preretinal granules can occur in FEVR, prompting a need for further investigation into their origins and connections to retinal vascular anomalies.

Article Abstract

Purpose: To report a rare clinical finding of preretinal granules associated with atypical familial exudative vitreoretinopathy (FEVR) and perform a review of the literature.

Observations: An asymptomatic 18-year-old male was referred for unilateral peripheral avascular retina evaluation in association with presumed FEVR. He was first noted to have white preretinal granules on fundus examination at five years of age. The lesions remained unchanged over the subsequent years. Genetic testing did not reveal a pathogenic or likely pathogenic variant in a known FEVR gene. A review of the literature revealed five other cases of FEVR with similar findings.

Conclusions And Importance: Literature review suggests preretinal granules may present rarely in FEVR. Negative genetic screening of known FEVR genes in our patient with atypical FEVR suggests either a molecularly distinct etiology supporting the rarity of this association with FEVR or, alternatively, the presence of granules in developmental retinal vascular anomalies that are not specific to FEVR. Future study and genetic testing is necessary to better understand the cause of these preretinal granules and the clinical manifestations of FEVR.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11019094PMC
http://dx.doi.org/10.1016/j.ajoc.2024.102051DOI Listing

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