Expanding the Phenotypic Spectrum of PRKD1 Gain-of-Function Syndrome: Congenital Heart Disease, Bilateral Carotid Dissections, and Ectodermal Dysplasia in an Adult Patient - Pedram Kharaziha; Klara Junker; Josefine Åhsberg; Antheia Kissopoulou (Genes, 2026)