[Criswick-Schepens syndrome -- familial exudative vitreoretinopathy. Report of six cases in two consanguineous families] | Canada Hyperbarics Skip to main content
Study Ophthalmologe 2004

[Criswick-Schepens syndrome -- familial exudative vitreoretinopathy. Report of six cases in two consanguineous families]

Alsheikheh A, Lieb W, Grehn F — Ophthalmologe, 2004

Tier 2, Indexed

Automatically imported from PubMed based on relevance criteria.

Summary

What Researchers Did

Researchers conducted a retrospective analysis of six cases of familial exudative vitreoretinopathy (FEVR) in children from two Syrian families with close genetic ties, examining their specific eye abnormalities.

What They Found

The six patients, aged between 3.5 and 13 years, presented with visual acuity ranging from light perception to 0.4 and various bilateral fundus changes. Key findings included papillary, macular, and retinal temporal traction in 11 eyes, a fibrovascular mass in 11 eyes, and a retinal fold in 7 eyes. Other abnormalities observed were vitreoretinal traction in 5 eyes, subretinal exudation in 2 eyes, and temporal or total tractional retinal detachment in 2 eyes.

What This Means for Canadian Patients

This study helps doctors better understand the diverse eye changes associated with familial exudative vitreoretinopathy (FEVR), a hereditary condition. Recognizing these specific fundus abnormalities is important for accurate diagnosis and for distinguishing FEVR from other similar pediatric eye diseases.

Canadian Relevance

No direct Canadian connection identified. This study describes a hereditary eye condition and does not involve hyperbaric oxygen therapy, nor does it cover a Health Canada-recognized indication for HBOT.

Study Limitations

The study's findings are limited by its retrospective design and small number of cases from specific consanguineous families.

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Study Details

Study Type Study
Category Ocular / Retinal
Source Pubmed
PubMed ID 15067562
Year Published 2004
Journal Ophthalmologe
MeSH Terms Adolescent; Child; Child, Preschool; Consanguinity; Female; Germany; Humans; Infant, Newborn; Male; Ophthalmoscopy; Pedigree; Phenotype; Retina; Retinal Degeneration; Retinal Detachment; Retinopathy of Prematurity; Syndrome; Syria; Visual Acuity; Vitreoretinopathy, Proliferative

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Disclaimer: This study summary is provided for informational and educational purposes only. It does not constitute medical advice. The information presented reflects the findings of the original research authors and may not represent the views of Canada Hyperbarics. Always consult a qualified healthcare professional before making treatment decisions.