Ovotesticular disorder of sex development (OTDSD) is a rare condition and defined as the presence of ovarian and testicular tissue in the same individual. Most of patients with OTDSD have female internal genital organs. In this report, we present a case in which, we demonstrated prostate tissue using endoscopic and radiologic methods in a 46-XX, sex determining region of the Y chromosome negative male phenotypic patient, with no female internal genitalia. Existence of prostate in an XX male without SRY is rarely seen and reveals a complete male phenotype. This finding is critical to figure out what happens in embryonal period.
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http://dx.doi.org/10.1111/j.1439-0272.2009.00945.x | DOI Listing |
Front Surg
December 2024
Department of Burn and Plastic Surgery, West China Hospital, Sichuan University, Chengdu, China.
Background: Ovotesticular disorder of sex development is a rare form of disorder of sex development that manifests as ovotestis in individuals. The precise diagnosis and the choice of surgical procedures are still in conflict condition due to the rarity of the disease, diverse clinical presentations, and the lack of evidence-based medical studies on postoperative outcomes.
Case Presentation: We present a 46, XX ovotesticular disorder of sex development case, aged 19, with Prader stage IV virilization who underwent feminizing genitoplasty surgery.
Can Vet J
November 2024
Centre de Diagnostic Vétérinaire de l'Université de Montréal (CDVUM) (St-Jean, Gagnon) and Swine and Poultry Infectious Diseases Research Center (CRIPA-FRQ) (Charreton-Sanford, Pesant, Gagnon), 3200 Rue Sicotte, Saint-Hyacinthe, Quebec J2S 2M2; Centre de Recherche en Reproduction et Fertilité, Université de Montréal, Saint-Hyacinthe, Quebec J2S 7C6 (St-Jean, Zamberlam, Boyer); MAPAQ - Direction Générale de la Santé Animale et de l'Inspection des Aliments, 5130 Boul. Guillaume-Couture, Lévis, Quebec G6V 9L4 (Beaudoin).
Cureus
October 2024
Cellular Biology and Anatomy, Louisiana State University Health Sciences Center, Shreveport, USA.
Turner syndrome is a chromosomal disorder affecting females characterized by the partial or complete absence of one X chromosome. The pathogenesis of Turner syndrome primarily arises from chromosomal nondisjunction during gametogenesis, leading to various genotypic presentations. The most common genotype is 45, XO, representing a monosomy of the X chromosome.
View Article and Find Full Text PDFGynecol Oncol Rep
December 2024
Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, Medical College of Georgia at Augusta University, 1120 15th Street, Augusta, GA 30912, USA.
Cureus
July 2024
Medical Genetics and Oncogenetics Laboratory, Hassan II University Hospital, Fez, MAR.
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