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:: Volume 21, Issue 1 (Iranian Journal of Ophthalmology 2009) ::
2009, 21(1): 65-69 Back to browse issues page
Proteus Syndrome: A Case Report of General and Ophthalmic Findings
Ahmad Mirshahi Dr., S-Mehrdad Mohammadi Dr. *, Arash MirMohammadSadeghi Dr.
, mmohamadi@tums.ac.ir
Abstract:   (10462 Views)

An 18-year-old girl fulfilled the diagnostic criteria for the Proteus syndrome (PS). Here we report our findings in comprehensive general physical and ocular examination and review the literature focused on clinical manifestations and differential diagnoses. The patient had ‘mild’ involvement of the ophthalmic apparatus: absent foveal reflex, cataract, and abnormal retinal vessels, which in the context of similar reports on ocular manifestations is an indication of wide polymorphism of the condition. Dermatologists, geneticists, and ophthalmologists should be aware of this disorder when they are consulted for the diagnosis of hamartomatous dysplasia conditions.

 

Iranian Journal of Ophthalmology 200921(1):65-69 © 2009 by the Iranian Society of Ophthalmology
Keywords: Proteus Syndrome, Absent Foveal Reflex (Macular Hypoplasia), Cataract, Abnormal Retinal Vessels
Full-Text [PDF 199 kb]   (2915 Downloads)    
Type of Study: Case report | Subject: General
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Mirshahi A, Mohammadi S, MirMohammadSadeghi A. Proteus Syndrome: A Case Report of General and Ophthalmic Findings. Iranian Journal of Ophthalmology. 2009; 21 (1) :65-69
URL: http://irjo.org/article-1-211-en.html


Volume 21, Issue 1 (Iranian Journal of Ophthalmology 2009) Back to browse issues page
مجله چشم پزشکی ایران Iranian Journal of Ophthalmology
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