Ophthalmological manifestations in a cohort of Cowden syndrome patients in a large tertiary healthcare system.

چکیده

Cowden syndrome (CS) is a rare genetic disorder caused by mutations in the PTEN gene associated with multisystem hamartomas and predisposition to malignancies. Although ocular involvement has been reported in case studies, systematic data are lacking. This study aimed to evaluate the prevalence,…

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موضوعات مرتبط

• رتینوپاتی نارسی
• چشم پزشکی کودکان