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Feyza Çalış Karanfil

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Oct 2026

Potocki-Shaffer syndrome associated with Brown syndrome: expansion of the ocular phenotype in a child with an 11p11.2-p11.12 deletion.

PURPOSE To describe the first reported case of Potocki-Shaffer syndrome (PSS) associated with Brown syndrome and to expand the ocular phenotype of this rare contiguous gene deletion syndrome. METHODS Retrospective case report with multidisciplinary ophthalmologic, neurologic, radiologic, and genetic evaluation over a...

Feyza Çalış Karanfil, Sabiha Güngör Kobat, Pınar Bingol Kiziltunc et al. · 0 citations

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