Wyburn-Mason syndrome

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Abstract

In the article, a description of a clinical case of an extremely rare isolated ophthalmic form of the Wyburn-Mason syndrome is presented. Etiology, pathogenesis, clinical picture, and diagnostic criteria of this disease are also described.

About the authors

Yuriy S. Astakhov

Academician I.P. Pavlov First St. Petersburg State Medical University

Author for correspondence.
Email: astakhov73@mail.ru

MD, PhD, DMedSc, professor

Russian Federation, Saint Petersburg

Svetlana G. Belekhova

Academician I.P. Pavlov First St. Petersburg State Medical University

Email: beleksv@yandex.ru

MD, assistant

Russian Federation, Saint Petersburg

Aida A. Shakhnazarova

Diagnostic center № 7 (ophthalmological) for adults and children

Email: beleksv@yandex.ru

MD, PhD

Russian Federation, Saint Petersburg

Andranik Yu. Ovnanyan

Academician I.P. Pavlov First St. Petersburg State Medical University

Email: ovnanyan@yandex.ru

MD, assistant. Ophthalmology Department

Russian Federation, Saint Petersburg

References

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Supplementary files

Supplementary Files
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1. JATS XML
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2. Fig. 1. Fundus photo: a lot of enlarged convoluted blood vessels resembling tangled worms

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3. Fig. 2. Optical coherence tomography: increased neuroepithelium thickness in the vascular loops area, vessels at the neuroepithelium inner layers level (white arrows), areas of the retinal pigment epithelium destruction

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4. Fig. 3. Fluorescein angiography: a – early venous phase (28 seconds); b – recirculation phase (12 minutes); c – capillary nonperfusion area in the late phase at the far periphery in the upper-outer quadrant. Description in the text

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5. Fig. 4. Indocyanine green angiography: a – early phase (38 seconds); b – late phase (12 minutes)

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Copyright (c) 2017 Astakhov Y.S., Belekhova S.G., Shakhnazarova A.A., Ovnanyan A.Y.

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This work is licensed under a Creative Commons Attribution 4.0 International License.
 


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