*  Sterilitätsabklärung vor tubenchirurgischen Eingriffen | SpringerLink
Coulam CB (1982) Premature gonadal failure. Fertil Steril 38/6: 645-655PubMedGoogle Scholar ... Bei etwa 15-20% aller Ehepaare mit Kinderwunsch ist sie bei beiden Partnern zu suchen, und etwa 10% fallen in den Bereich der ... Aleem FA (1981) Familial 46 XX gonadal dysgenesis. Fertil Steril 35/3: 317-320PubMedGoogle Scholar ...
  https://link.springer.com/chapter/10.1007/978-3-642-59833-3_5
*  Back burning sensation and Skin symptoms - Symptom Checker - check medical symptoms at RightDiagnosis
XX Gonadal dysgenesis epibulbar dermoid. 8. 4p16.3 deletion. 9. Aantibodies anti-FVIIIc syndrome. 10. Aarskog Syndrome. More ...
  http://wrongdiagnosis.com/cosymptoms/back-burning-sensation/skin-symptoms.htm
*  Fertility symptoms - RightDiagnosis.com
XX Gonadal dysgenesis epibulbar dermoid - hypogonadism *46,XX testicular disorder of sex development - reduced hormone ... Gonadal dysgenesis ... infertility*Gonadal dysgenesis Turner type ... infertility*Grahmann's syndrome ... hypogonadism* ... XX Gonadal dysgenesis epibulbar dermoid ... hypogonadism*46,XX testicular disorder of sex development ... reduced hormone ... XY Gonadal Dysgenesis, Complete, SRY-Related - infertility *47,XXX syndrome - infertility *more causes...» See full list of 370 ...
  http://www.rightdiagnosis.com/sym/fertility_symptoms.htm
*  XX gonadal dysgenesis - Wikipedia
In contrast XX gonadal dysgenesis has a normal female chromosome situation. Another type of XX gonadal dysgenesis is known as ... In both sexes sensorineural deafness occurs but in females ovarian dysgenesis also occurs. XX gonadal dysgenesis is a type of ... The term "pure gonadal dysgenesis" (PGD) has been used to distinguish a group of patients from gonadal dysgenesis related to ... Thus XX gonadal dysgenesis is also referred to as PGD, 46 XX, and XY gonadal dysgenesis as PGD, 46,XY or Swyer syndrome. ...
  https://en.wikipedia.org/wiki/XX_gonadal_dysgenesis
*  Ovotesticular Disorder of Sexual Development Treatment & Management: Medical Care, Surgical Care, Consultations
Dysgerminoma and gonadal dysgenesis in a 46,XX female with no evidence of Y chromosomal DNA. Gynecol Oncol. 1995 Jun. 57(3):423 ... XX Maleness and XX true hermaphroditism in SRY-negative monozygotic twins: additional evidence for a common origin. J Clin ... The role of the sex determining region of the X chromosome (SRY) in the etiology of 46XX true hermaphroditism. Hum Genet. 1992 ... The role of sexual related Y gene detection in the diagnosis of patients with gonadal dysgenesis. Chin Med J (Engl). 2001 Feb. ...
  https://emedicine.medscape.com/article/256289-treatment
*  Belching and Diarrhea and Puberty symptoms - Symptom Checker - check medical symptoms at RightDiagnosis
XX Gonadal dysgenesis epibulbar dermoid. 4. Abdominal Cancer. 5. Abdominal abscess. 6. Abdominal conditions. 7. Acanthocytosis ...
  http://symptoms.rightdiagnosis.com/cosymptoms/belching/diarrhea/puberty-symptoms.htm
*  Headache in children and Skin symptoms - Symptom Checker - check medical symptoms at RightDiagnosis
XX Gonadal dysgenesis epibulbar dermoid. 8. 4p16.3 deletion. 9. Aantibodies anti-FVIIIc syndrome. 10. Aarskog Syndrome. More ... Headache in children and Skin symptoms and Abdominal symptoms (20 causes). *Headache in children and Skin symptoms and ...
  http://symptoms.rightdiagnosis.com/cosymptoms/headache-in-children/skin-symptoms.htm
*  Nausea and Skin symptoms - Symptom Checker - check medical symptoms at RightDiagnosis
XX Gonadal dysgenesis epibulbar dermoid. A rare disorder characterized by gonad abnormalities and an eye disorder called ...
  http://symptoms.rightdiagnosis.com/cosymptoms/nausea/skin-symptoms-desc.htm
*  Leg swelling and Skin symptoms - Symptom Checker - check medical symptoms at RightDiagnosis
XX Gonadal dysgenesis epibulbar dermoid. 8. 4p16.3 deletion. 9. Aagenaes syndrome. 10. Aantibodies anti-FVIIIc syndrome. More ...
  http://symptoms.rightdiagnosis.com/cosymptoms/leg-swelling/skin-symptoms.htm
*  Follicle-stimulating hormone receptor - Wikipedia
Women with 46 XX gonadal dysgenesis experience primary amenorrhea with hypergonadotropic hypogonadism. There are forms of 46 xx ... gonadal dysgenesis wherein abnormalities in the FSH-receptor have been reported and are thought to be the cause of the ...
  https://en.wikipedia.org/wiki/Follicle-stimulating_hormone_receptor
*  GENTAUR antibody-antibodies.com The Marketplace for Antibodies
XX gonadal dysgenesis.. Orphanet; 64739; Ovarian hyperstimulation syndrome.. Orphanet; 619; Primary ovarian failure.. PharmGKB ... DISEASE: Ovarian dysgenesis 1 (ODG1) [MIM:233300]: An autosomal. recessive disease characterized by primary amenorrhea, ... 20]. VARIANT ODG1 VAL-189.. PubMed=9851774; DOI=10.1210/jcem.83.12.5306;. Jiang M., Aittomaeki K., Nilsson C., Pakarinen P., ... DOMAIN 18 46 LRRNT.. REPEAT 49 72 LRR 1.. REPEAT 73 97 LRR 2.. REPEAT 98 118 LRR 3.. REPEAT 119 143 LRR 4.. REPEAT 144 169 LRR ...
  http://www.antibody-antibodies.com/gene.php?title_uniprot=Follicle-stimulating+hormone+receptor+%28FSH-R%29+%28Follitropin+receptor%29&uniprot_id=P23945
*  Orange Colour Information
... xx gonadal dysgenesis epibulbar dermoid. The information on this website is provided for information purposes only and is not ...
  http://www.dianamossop.com/tabid/243/col/8/colour/orange.aspx
*  Aetiological bases of 46,XY disorders of sex development in the Hong Kong Chinese population | HKMJ
XX gonadal dysgenesis phenotype variability in multiple members of an affected kindred. Horm Res Paediatr 2012;78:119-26. ... Gonadal malignancy was rare in our series, probably because gonadectomy was performed early in life when the decision of female ... Objective: Disorders of sex development are due to congenital defects in chromosomal, gonadal, or anatomical sex development. ... 9. Bangsbøll S, Qvist I, Lebech PE, Lewinsky M. Testicular feminization syndrome and associated gonadal tumors in Denmark. Acta ...
  http://www.hkmj.org/abstracts/v21n6/499.htm
*  Featured Stories | The Addi and Cassi Fund - Niemann Pick Type C - Part 2
Gonadal dysgenesis Turner type, Gonadal dysgenesis XY type associated anomalies, Gonadal dysgenesis XX type, Goniodysgenesis ... Corpus callosum dysgenesis cleft spasm, Corpus callosum dysgenesis hypopituitarism, Corpus callosum dysgenesis X-linked ... Renal tubular dysgenesis, Renal tubulopathy diabetes mellitus and cerebellar ataxia due to duplication of mitochondrial DNA, ... Twenty-nail dystrophy, Twin twin transfusion syndrome, Tylosis, Type 1 plasminogen deficiency, Typhoid fever, Typhus, Tyrosine- ...
  http://addiandcassi.com/category/featured-stories/page/2/
*  Chromosome 23 deletion - Tips and Tricks From Doctors
Sex chromosomes: XX female. XY male. Great wikipedia question. Get a more detailed answer › ... 46: May have pieces that are switched aroung causing different phenotypes, either good or bad. ...Read more ... Their verbal and performance iqs are 15 to 20 points lower than those of their siblings. These women do not appear to be at ... Hermaphroditism can also occur in 46 xx individuals with a fragment of a y chromosome. ...Read more ...
  https://www.healthtap.com/topics/chromosome-23-deletion
*  XY gonadal dysgenesis - Wikipedia
... and XX gonadal dysgenesis as PGD, 46,XX. Patients with PGD have a normal karyotype but may have defects of a specific gene on a ... Types include: There are several forms of gonadal dysgenesis. The term "pure gonadal dysgenesis" (PGD) has been used to ... Gonadal dysgenesis Stoicanescu D, Belengeanu V, et al. (2006). "Complete Gonadal Dysgenesis With XY Chromosomal Constitution". ... and hence is part of a class of conditions termed gonadal dysgenesis. There are many forms of gonadal dysgenesis. Swyer ...
  https://en.wikipedia.org/wiki/XY_gonadal_dysgenesis
*  Primary Ovarian Insufficiency - Gynecology and Obstetrics - Merck Manuals Professional Edition
XX or 45,X/47,XXX]) or mixed gonadal dysgenesis) ... Gonadal dysgenesis secondary to genetic defects (eg, Turner ... A pregnancy test is done, and serum FSH and estradiol levels are measured weekly for 2 to 4 wk; if FSH levels are high (> 20 ... Confirm the diagnosis by measuring FSH (which is high, usually > 30 mIU/mL) and estradiol (which is low, usually < 20 pg/mL). ... Turner syndrome (45,X or mosaic 45,X/46,XX or 45,X/47,XXX) ... 20 pg/mL), ovarian insufficiency is confirmed. Then, further ...
  http://www.merckmanuals.com/en-ca/professional/gynecology-and-obstetrics/menstrual-abnormalities/primary-ovarian-insufficiency
*  Delayed Recognition of Disorders of Sex Development (DSD): A Missed Opportunity for Early Diagnosis of Malignant Germ Cell...
XX DSD, and sex chromosomal DSD. Within these subgroups, patients, with gonadal dysgenesis (GD) and hypovirilization with ... DSD patients with gonadal dysgenesis or hypovirilization, containing part of the Y chromosome (GBY), have an increased risk for ... One family showed two sisters with XY sex reversal, gonadal dysgenesis, and GB, and the other family included one daughter with ... partial gonadal dysgenesis [1]. A summary of the various actions and observations in time is schematically shown in Figure 3(h ...
  https://www.hindawi.com/journals/ije/2012/671209/
*  List of MeSH codes (C13) - Wikipedia
... xx MeSH C13.371.820.700.842.309.388 --- gonadal dysgenesis, 46,xy MeSH C13.371.820.700.842.309.391 --- gonadal dysgenesis, ... gonadal dysgenesis MeSH C13.371.820.700.842.309.193 --- gonadal dysgenesis, 46, ...
  https://en.wikipedia.org/wiki/List_of_MeSH_codes_(C13)
*  List of MeSH codes (C19) - Wikipedia
... xx MeSH C19.391.775.309.388 --- gonadal dysgenesis, 46,xy MeSH C19.391.775.309.391 --- gonadal dysgenesis, mixed MeSH C19.391. ... gonadal dysgenesis MeSH C19.391.775.309.193 --- gonadal dysgenesis, 46, ...
  https://en.wikipedia.org/wiki/List_of_MeSH_codes_(C19)