• Source: XX gonadal dysgenesis

XX gonadal dysgenesis is a type of female hypogonadism in which the ovaries do not function 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.




Presentation






= Related conditions

=
XX gonadal dysgenesis is related to the Swyer syndrome in as much as both conditions have the same phenotype and clinical issues; however in Swyer syndrome the karyotype is 46,XY, and thus gonadectomy is recommended.
In Turner syndrome there is a demonstrable abnormality in or absence of one of the sex chromosomes that is the cause of the development of gonadal dysgenesis. In contrast XX gonadal dysgenesis has a normal female chromosome situation.
Another type of XX gonadal dysgenesis is known as 46,XX gonadal dysgenesis epibulbar dermoid, which follows the similar symptoms as the regular syndrome, though it also shows signs of epibulbar dermoid (eye disorder). It has been suggested to be a new type of syndrome.




Pathogenesis


The cause of the condition is often unclear.
In cases without hearing involvement, some implicated genes are:

FOXL2, NOBOX, and FIGLA, related to ovarian development. FOXL2 mutation can cause Blepharophimosis, ptosis, epicanthus inversus syndrome, which affects the eyes at the same time.
FSH receptor, related to signaling. Autosomal recessive.
BMP15, associated with X-linked form.
EIF2B2, EIF2B4, and EIF2B5, responsible for protein production (see eIF2).
PSMC3IP, autosomal recessive; mutation reduces estrogen-induced transcription of this gene.
Various genes involved in steroidogenesis
In cases with hearing involvement (Perrault syndrome), the following genes are implicated:

LARS2 and HARS2, two mitochondrial tRNA synthetase genes
HSD17B4, involved in steroidogenesis and fatty acid metabolism
TWNK, the mitochondrial helicase
ERAL1, a mitochondrial rRNA chaperone
CLPP, a mitochondrial protease
RMND1, a protein involved in mitochondrial translation; causes kidney problems on top of classical Perrault symptons. Three cases are reported as of 2020.
Apparently either the germ cells do not form or interact with the gonadal ridge or undergo accelerated atresia so that at the end of childhood only a streak gonad is present, unable to induce pubertal changes. As girls' ovaries produce no important body changes before puberty, there is usually no suspicion of a defect of the reproductive system until puberty fails to occur.
Familial cases of XX gonadal dysgenesis are on record.




Diagnosis


Because of the inability of the streak gonads to produce sex hormones (both estrogens and androgens), most of the secondary sex characteristics do not develop. This is especially true of estrogenic changes such as breast development, widening of the pelvis and hips, and menstrual periods. Because the adrenal glands can make limited amounts of androgens and are not affected by this syndrome, most of these girls will develop pubic hair, though it often remains sparse.
Evaluation of delayed puberty usually reveals the presence of pubic hair, but elevation of gonadotropins, indicating that the pituitary is providing the signal for puberty but the gonads are failing to respond. The next steps of the evaluation usually include checking a karyotype and imaging of the pelvis. The karyotype reveals XX chromosomes and the imaging demonstrates the presence of a uterus but no ovaries (the streak gonads are not usually seen by most imaging). At this point it is usually possible for a physician to make a diagnosis of XX gonadal dysgenesis.




Treatment


The consequences to the girl with XX gonadal dysgenesis:

Her gonads cannot make estrogen, so her breasts will not develop and her uterus will not grow and menstruate until she is given estrogen. This is often given through the skin now.
Her gonads cannot make progesterone, so her menstrual periods will not be predictable until she is given a progestin, still usually as a pill.
Her gonads cannot produce eggs so she will not be able to conceive children naturally. A woman with a uterus but no ovaries may be able to become pregnant by implantation of another woman's fertilized egg (embryo transfer).




History


In 1951, Perrault reported the association of gonadal dysgenesis and deafness, now called Perrault syndrome.




See also


Sex chromosome anomalies
Gonadal dysgenesis




References






External links

Kata Kunci Pencarian:

• Gonadal dysgenesis
• XX gonadal dysgenesis
• XY gonadal dysgenesis
• XX
• Gonadal agenesis
• Sex chromosome anomalies
• XX male syndrome
• Hypergonadotropic hypogonadism
• Turner syndrome
• Unilateral ovarian agenesis