Klippel–Trenaunay syndrome presenting with bilateral chronic central serous chorioretinopathy: a case report
Alisina Eghbalnia, Romina Dadkhah, Hamid Riazi‐Esfahani, Elias Khalili Pour
BACKGROUND: Klippel-Trenaunay syndrome (KTS) is a rare congenital vascular disorder characterized by capillary malformations, venous and/or lymphatic malformations, and asymmetric limb overgrowth. It results from somatic activating mutations in the PIK3CA gene, leading to dysregulated vascular development. While primarily affecting the skin …
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Journal of Medical Case Reports