Frasier Syndrome Market: Emerging Therapeutic Solutions for Rare Genetic Disorders up to 2033
Frasier Syndrome is a rare genetic disorder characterized by a mutation in the WT1 gene, which plays a critical role in kidney and reproductive system development. This syndrome primarily affects the kidneys and gonads, leading to progressive kidney disease (often nephrotic syndrome) and gonadal dysgenesis, which can result in ambiguous genitalia or underdeveloped reproductive organs. The disorder usually manifests during early childhood or adolescence, with symptoms including proteinuria (excess protein in the urine), chronic kidney failure, and an increased risk of developing certain types of cancer, such as gonadoblastoma.