dysgenesis$23473$ - ορισμός. Τι είναι το dysgenesis$23473$
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Τι (ποιος) είναι dysgenesis$23473$ - ορισμός

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

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
XX gonadal dysgenesis         
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.
Anterior segment mesenchymal dysgenesis         
HUMAN DISEASE
Anterior Segment Dysgenesis; Peters anomaly; Peter's anomaly; Peters' anomaly; Anterior chamber cleavage syndrome; Mesodermal dysgenesis of cornea; Anterior segment dysgenesis
Anterior segment mesenchymal dysgenesis, or simply anterior segment dysgenesis (ASD), is a failure of the normal development of the tissues of the anterior segment of the eye. It leads to anomalies in the structure of the mature anterior segment, associated with an increased risk of glaucoma and corneal opacity.

Βικιπαίδεια

XX gonadal dysgenesis

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. Estrogen and progesterone therapy is usually then commenced. Some cases are considered a severe version of premature ovarian failure where the ovaries fail before puberty.

Some forms of XX gonadal dysgenesis occurs with sensorineural deafness. This type is also known as Perrault syndrome, an autosomal recessive disease affecting both sexes. Males present only with the deafness.

The term "pure gonadal dysgenesis" (PGD) has been used to distinguish a group of patients from gonadal dysgenesis related to Turner syndrome. In the latter a distinct chromosomal aberration is present, while in PGD the chromosomal constellation is either 46,XX or 46,XY. Thus XX gonadal dysgenesis is also referred to as PGD, 46 XX, and XY gonadal dysgenesis as PGD, 46,XY or Swyer syndrome. Patients with PGD have a normal chromosomal constellation but may have localized genetic alterations.