Results 91 to 100 of about 167,060,252 (161)

Gender Dysphoria and Gender Change in Disorders of Sex Development/Intersex Conditions: Results From the dsd-LIFE Study

, 2018
© 2018 International Society for Sexual Medicine Background: Information on the psychosexual outcome of individuals with disorders of sex development (DSDs) and intersex conditions is of great importance for sex assignment at birth of newborns with DSD ...
Claahsen-van der Grinten, Hedi, Reisch, Nicole, Köhler, Birgit, Roehle, Robert, Slowikowska-Hilczer, Jolanta, Arlt, Wiebke, Paris, Francoise, Pienkowski, Catherine, Sultan, Charles, Bouvattier, Claire, de Vries, Annelou L.C., de la Perriere, Aude Brac, Szarras-Czapnik, Maria, Richter-Unruh, Annette, Cohen-Kettenis, Peggy T., Nordenström, Anna, Kreukels, Baudewijntje P.C., Thyen, Ute, Wiesemann, Claudia   +18 more
core   +1 more source

The I-DSD network (International Disorders of Sex Development)

, 2013
The I-DSD Network The I-DSD network (International Disorders of Sex Development) is a 5 year MRC funded initiative to support the development of an International DSD registry and network of clinical and research partners.
Claudia Wiesemann, John Achermann, Olaf Hiort, John Watt, Ian Ford, Martina Rodie, Feyza Darendeliler, Berenice Mendonca, Project Management Group Faisal Ahmed, BALSAMO, ANTONIO, Jillian Bryce, David Sandberg, Richard Sinnott, Jipu Jiang, Ellie Magritte, Ieuan Hughes   +15 more
core   +1 more source

Ovotesticular disorder of sex development with unusual karyotype: patient report

, 2015
Background: Ovotesticular disorder of sex development (OT-DSD) (true hermaphroditism) is an anatomopathological diagnosis based on the findings of testicular and ovarian tissues in the same subject, in the same gonad (ovotestis), or in separate gonads ...
Maciel-Guerra, Andrea Trevas, Paula, Georgette Beatriz, Miranda, Marcio Lopes, Guaragna-Filho, Guilherme, Sewaybricker, Leticia Esposito, Ribeiro Andrade, Juliana Gabriel, Guerra-Junior, Gil   +6 more
core   +1 more source

Post-pubertal presentation of 46XY disorders of sex development: A case report

Bangabandhu Sheikh Mujib Medical University Journal
Not ...
Md. Shafiquzzaman, Md. Saiful Islam, Md. Nazrul Islam   +2 more
doaj   +1 more source

Pull-through vaginoplasty with anterior sagittal transrectal approach in high confluence urogenital sinus and 46XX, DSD: A case report and literature review

Urology Case Reports
We report our experience of pull-through vagina with anterior sagittal approach of high.UGS in 46,XX disorder of sex development (DSD). Rare case of 4-year-old girl presented with UGS and 46,XX DSD with the chief complaint of purulent urination since 2 ...
Angger Satria Pamungkas, Gerhard Reinaldi Situmorang, Muhammad Ridha, Irfan Wahyudi   +3 more
doaj   +1 more source

Genetic Characterization and Multidisciplinary Management of Complete Androgen Insensitivity Syndrome: Unveiling a Novel AR Mutation

Clinical Case Reports
A novel AR frameshift mutation (c.2023_2035del) was identified in a 17‐year‐old phenotypic female with Complete Androgen Insensitivity Syndrome (CAIS). This report emphasizes the necessity of molecular characterization and multidisciplinary management to
Maria Francesca Astorino, Serena Scalise, Chiara Di Bella, Maria Angela La Rosa, Basilia Piraino, Marco Calabrò, Mattia Gentile, Rosaria Maddalena Ruggeri, Emanuela Esposito, Silvana Briuglia, Salvatore Cannavò   +10 more
doaj   +1 more source

46 XX Ovotesticular Disorder of Sex Development with Gonadotropin-Releasing Hormone Receptor, Autosomal Recessive Heterozygous Missense Mutation and Autosomal Dominant Heterozygous Missense Mutation of the PROKR2 Gene: A Case Report

Global Medical Genetics
True hermaphroditism is a disorder of sex development (DSD), accounting for less than 5% of all DSD cases, defined by the simultaneous presence of testicular tissue and ovarian tissue in the same individual.
Francesca Peranzoni, Roberto De Castro, Emilio Merlini, Yen Le Nguyen   +3 more
doaj   +1 more source

Disorders of Sex Development (DSD): networking and standardization considerations

, 2015
Syndromes resulting in Disorders of Sex Development (DSD) are individually rare. Historically, this fact has hindered both clinical research and the delivery of evidence-based care.
Callens, Nina, Sandberg, David, Wisniewski, Amy   +2 more
core   +1 more source

Familial 46, XY Disorder of Sexual Development identified in a Ph+BCR::ABL1P210+ Acute Lymphoblastic Leukemia septuagenarian female with RCBTB2::LPAR6 fusion gene: a case report

Frontiers in Oncology
BackgroundFamilial 46, XY Disorder of Sexual Development (DSD) was discovered in a Ph+, BCR::ABL1P210+ Acute Lymphoblastic Leukemia (ALL) female with RCBTB2::LPAR6 fusion gene. Siblings developing 46, XY DSD are extremely rare.
Lingling Wang, Conglin Xi, Xinyu Zheng, Yongfen Huang, Hao Xu, Yuqing Miao, Yuexin Cheng   +6 more
doaj   +1 more source

46, XX disorder of sexual development associated with mixed germ cell tumor of the prostate: a rare case report

BMC Urology
Background Extragonadal germ cell tumors originating from the prostate are exceptionally rare. To the best of our knowledge, there have been no reported cases of mixed germ cell tumors in individuals with 46 XX disorder of sex development. In this study,
Changrong Wang, Jiangli Du, Xueping Xiang, Yuyong Wang, Jingjing Xiang, Qiaoping Xu   +5 more
doaj   +1 more source