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  Vol. 127 No. 12, December 2009 TABLE OF CONTENTS
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  Ophthalmic Molecular Genetics
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Clinical Presentation and Genetic Correlation of Patients With Mutations Affecting the FZD4 Gene

Kimberly A. Drenser, MD, PhD; Wendelin Dailey, BS; Anand Vinekar, MD; Kunal Dalal, MD; Antonio Capone Jr, MD; Michael T. Trese, MD

Arch Ophthalmol. 2009;127(12):1649-1654.

Objective  To correlate the ophthalmic findings of patients with pediatric vitreoretinopathies with mutations occurring in the FZD4 gene.

Methods  A total of 123 patients diagnosed with autosomal-dominant familial exudative vitreoretinopathy (AdFEVR) or retinopathy of prematurity (ROP) and 42 control patients were enrolled in the study. Diagnoses were based on retinal findings at each patient's first examination or during ROP screening. Genomic DNA was isolated and polymerase chain reaction and direct sequencing of the FZD4 gene performed.

Results  FZD4 gene mutations were discovered in 13 of the 123 (10.6%) patients. Nine of the 63 patients with AdFEVR (14.3%) has mutations in the FZD4 gene. Four heterozygous mutations were identified: C117R, C181Y, Q505X, and P33S/P168S. Four of the 60 patients with ROP (6.7%) have a double missense mutation P33S/P168S that was also found in the patients with FEVR. No other FZD4 mutations were found in the patients with ROP. Additionally, patients expressing the double mutation had clinical presentations that overlapped, making it difficult to assign a definitive diagnosis. None of the mutations found in the patients with FEVR or ROP were seen in the control chromosomes.

Conclusion  Mutations occurring in the FZD4 gene affect patients diagnosed with both FEVR and ROP. The clinical picture often overlaps and may require a detailed birth and family history for diagnosis. Genetic testing confirms inherited vitreoretinopathy and helps direct clinical management.

Clinical Relevance  Patients diagnosed with ROP may have a mutation in the FZD4 gene and display characteristics consistent with FEVR. Analysis of the FZD4 gene should be considered.


Author Affiliations: Associated Retinal Consultants, William Beaumont Hospital, Royal Oak, Michigan (Drs Drenser, Dalal, Capone, and Trese, and Ms Dailey); and the Department of Ophthalmology, Advanced Eye Center, Postgraduate Institute of Medical Education and Research, Chandigarh, India (Dr Vinekar).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease
Robitaille et al.
Br J Ophthalmol 2011;95:574-579.
ABSTRACT | FULL TEXT  

Novel Frizzled-4 Gene Mutations in Chinese Patients With Familial Exudative Vitreoretinopathy
Jia et al.
Arch Ophthalmol 2010;128:1341-1349.
ABSTRACT | FULL TEXT  





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