XY complete gonadal dysgenesis, also known as Swyer syndrome, is a condition resulting in a female phenotype in an individual with a 46,XY karyotype.

Swyer syndrome is when a person has XY (male) chromosomes and functional female genitalia (vulva). While XY chromosomes usually result in the development of a penis and scrotum, people with Swyer …

In Swyer syndrome, individuals have one X chromosome and one Y chromosome in each cell, which is the pattern typically found in boys and men; however, they have female reproductive structures. …

Nov 4, 2025 · Swyer syndrome, also known as complete gonadal dysgenesis (CGD), is a rare congenital disorder of sex development where a person has a 46, XY (male) karyotype but develops as a female.

Sep 18, 2019 · Learn about Swyer syndrome, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find resources and.

Mar 13, 2025 · Swyer syndrome, also known as pure gonadal dysgenesis 46 XY, is a genetic disorder of the sex chromosomes characterized by the absence of correlation between the sexual phenotype …

Gonadal dysgenesis, also known as 46XY gonadal dysgenesis and Swyer syndrome, is a condition where a baby's ovaries or testes (gonads) did not form the right way during pregnancy.

Swyer Syndrome is a genetic condition where individuals with XY chromosomes develop as females due to the underdevelopment or absence of functional gonads. It is characterized by a lack of …

May 19, 2025 · Swyer syndrome is a rare genetic disorder that affects sexual development and differentiation. Despite its rarity, understanding this condition is crucial for affected individuals, their …

Learn about the genetic causes, symptoms, and treatments for Swyer syndrome, including options for reproductive assistance.