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Article

WAGNER syndrome: anatomic, functional and genetic characterization of a Portuguese family.

Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie - 1 Jan 2018

Araújo Joana R, Tavares-Ferreira João, Estrela-Silva Sérgio, Rocha Paulo, Brandão Elisete, Faria Pedro Alves, Falcão-Reis Fernando, Rocha-Sousa Amândio

Abstract excerpt

PURPOSE: To report the clinical (anatomic and functional) and genetic findings of Wagner Syndrome (WS) in a Portuguese family. METHODS: Nine members of the family agreed to be examined. All had complete clinical eye examinations. The proband and selected patients underwent color fundus photography, spectral domain optical coherence tomography (SD-OCT), automatic static white-on-white computerized perimetry, and...

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Source

Identifiers

PMID: 29071374
DOI: 10.1007/s00417-017-3800-0

Genes

ERG
VCAN

Provenance

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