Search results
Frasier syndrome is a urogenital anomaly associated with the WT1 (Wilms tumor 1 gene) gene. [1] [2] [3] It was first characterized in 1964. [4] Presentation. Both males and females can have Frasier syndrome but their presentations can be different.
Frasier syndrome is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they may occur randomly when cells are dividing.
Jul 21, 2021 · Frasier syndrome is a rare disease that affects the kidneys and genitalia. Patients who have Frasier syndrome develop nephrotic syndrome (NS) featuring focal segmental glomerulosclerosis (FSGS) that is resistant to steroid treatment in early childhood.
Frasier syndrome is a rare genetic condition that causes kidney disease and gonadal dysgenesis in males. Learn about the symptoms, inheritance, genetics and resources of this condition.
Frasier syndrome. Suggest an update. Disease definition. A rare genetic, syndromic glomerular disorder characterized by the association of progressive glomerular nephropathy and 46,XY complete gonadal dysgenesis with a high risk of developing gonadoblastoma. ORPHA:347. Classification level: Disorder. Prevalence: <1 / 1 000 000.
Frasier syndrome is a rare disorder caused by mutations in the WT1 gene that affects the kidneys and the sex organs. Learn about the symptoms, diagnosis, treatment, and prognosis of this condition from various chapters and articles on ScienceDirect Topics.
Apr 30, 2020 · Frasier syndrome, Denys-Drash syndrome, and Meacham syndrome were originally described as distinct disorders on the basis of clinical findings but are now understood to represent a continuum of features caused by a WT1 heterozygous pathogenic variant. Given the extensive clinical overlap between these clinical diagnoses and molecular ...
