XX gonadal dysgenesis - definition. What is XX gonadal dysgenesis
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XX gonadal dysgenesis         
GONADAL DYSGENESIS THAT IS CHARACTERIZED BY THE LACK OF FUNCTIONAL OVARIES TO INDUCE PUBERTY IN AN OTHERWISE 46,XX FEMALE
Perrault syndrome; Gonadal dysgenesis, XX type; 46 xx gonadal dysgenesis epibulbar dermoid
XX gonadal dysgenesis is a type of female hypogonadism in which no functional ovaries are present to induce puberty in an otherwise normal girl whose karyotype is found to be 46,XX. With nonfunctional streak ovaries, she is low in estrogen levels (hypoestrogenic) and has high levels of FSH and LH.
Gonadal dysgenesis         
CONGENITAL DISORDER OF THE REPRODUCTIVE SYSTEM
Streak gonad; Streak gonads; Ovarian dysgenesis; Pure gonadal dysgenesis; Streaked ovaries; Streak ovaries; Streak ovary; Ovarian malformation; Testicular dysgenesis; Agonadism; Agonadal; Agonad
Gonadal dysgenesis is classified as any congenital developmental disorder of the reproductive system
XY gonadal dysgenesis         
GONADAL DYSGENESIS THAT IS CHARACTERIZED BY A NORMAL 46,XY KARYOTYPE ALONG WITH A PROGRESSIVE LOSS OF GERM CELLS ON THE DEVELOPING GONADS OF AN EMBRYO
Swyer's syndrome; XY Female; XY female syndrome; Gonadal dysgenesis, 46,xy; Gonadal dysgenesis, XY female type; Swyer syndrome; XY female
XY gonadal dysgenesis, also known as Swyer syndrome, is a type of hypogonadism in a person whose karyotype is 46,XY. Though they typically have normal female external genitalia, the person has functionless gonads, fibrous tissue termed "streak gonads", and if left untreated, will not experience puberty. Such gonads are typically surgically removed (as they have a significant risk of developing cancer). The typical medical treatment is hormone replacement therapy.