Familial ROSAH Syndrome Associated with the ALPK1 p.Thr237Ala Variant: Divergent Ocular Phenotypes and Partial Response to IL-6 Blockade.
PURPOSE To report phenotypic variability and treatment response in familial ROSAH syndrome associated with the ALPK1 p.Thr237Ala variant. METHODS Longitudinal observational familial case series of a mother-daughter pair with ALPK1-associated ROSAH syndrome. The daughter carried a heterozygous ALPK1 p.Thr237Ala varian...