Results 51 to 60 of about 10,963 (227)

Complete androgen insensitivity Syndrome: A rare case report

Asian Journal of Surgery, 2023
Xiao Xiao, Zhou Yang
doaj   +2 more sources

Genotype versus phenotype in families with androgen insensitivity syndrome [PDF]

, 2001
Androgen insensitivity syndrome encompasses a wide range of phenotypes, which are caused by numerous different mutations in the AR gene. Detailed information on the genotype/phenotype relationship in androgen insensitivity syndrome is ...
Assendelft, C. van, Boehmer, A.L., Brinkmann, A.O., Bruggenwirth, H.T., Brunner, H.G., Drop, S.L., Kleijer, W.J., Kwast, T.H. van der, Niermeijer, M.F., Oostdijk, W., Otten, B.J., Rouwé, C.W., Verleun-Mooijman, M.C.T., Vroede, M.A. de, Waelkens, J.J.   +14 more
core   +15 more sources

Challenges in laparoscopic gonadectomy for complete androgen insensitivity syndrome with nonpalpable inguinal glands. [PDF]

Int J Surg Case Rep
Takedomi R, Kurita T, Higashijima K, Hagimoto M, Higami S, Yoshino K.   +5 more
europepmc   +2 more sources

Complete Androgen Insensitivity Syndrome [PDF]

The Journal of Obstetrics and Gynecology of India, 2012
Complete androgen insensitivity syndrome (AIS) is a medical condition which affects the development of the genital and reproductive system. This raises some very uncomfortable issues about gender identity that are difficult to put into words. The first medical report on AIS was published in 1953 by J. M. Morris, an American gynecologist.
Hemant, Deshpande, Shilpa, Chaudhari, Shivani, Sharma   +2 more
openaire   +2 more sources

The challenges of androgen insensitivity syndrome

Archives of Medical Science, 2021
Androgen insensitivity syndrome (AIS) is an X-linked recessive genetic syndrome that occurs as result of an androgen receptor mutation; it affects the normal masculinization process in chromosomal male patients.
Bratu Ovidiu, Dragos R. Marcu, Dan L. D. Mischianu, Catalina Poiana, Camelia C. Diaconu, Simona G. Bungau, Delia M. Tit, Alin Cumpanas, Roxana Bohiltea   +8 more
doaj   +1 more source

COMPLETE ANDROGEN INSENSITIVITY SYNDROME: CASE REPORT COMPLETE ANDROGEN INSENSITIVITY SYNDROME

Revista Portuguesa de Endocrinologia, Diabetes e Metabolismo
Eduarda Zardin, Gabrielly Araújo, Katia Souto, Julia Souza, Lais Alvaristo   +4 more
openaire   +2 more sources

Challenges in the Diagnosis of XY Differences of Sexual Development

Medicina, 2022
Background: We report the clinical case of female patient with 46,XY difference of sexual development (DSD) and discuss the challenges in the differential diagnosis between complete gonadal dysgenesis (also called Swyer syndrome) and complete androgen ...
Žana Bumbulienė, Diana Bužinskienė, Greta Banuškevičienė, Evelina Šidlovska, Eglė Preikšaitienė, Algirdas Utkus   +5 more
doaj   +1 more source

Laparoscopic gonedectomy in a case of complete androgen insensitivity syndrome

Journal of Human Reproductive Sciences, 2014
Complete Androgen insensitivity syndrome is a disorder of hormone resistance characterized by a female phenotype in an individual with an XY karyotype. The pathogenesis of CAIS involves a defective androgen receptor gene located on X-chromosome at Xq11 ...
G Bhaskararao, Y Himabindu, Samir Ranjan Nayak, M Sriharibabu   +3 more
doaj   +1 more source

Laparoscopy in inguinal hernia and complete androgen insensitivity syndrome in children. Whether and when to remove the gonads because of cancer?

Studia Medyczne, 2016
Androgen insensitivity syndrome (CAIS) – also called Morris syndrome, formerly known as testicular feminisation syndrome – is a congenital disorder of sex development caused by various mutations in the gene encoding the androgen receptor.
Przemysław Wolak
doaj   +1 more source

Androgen receptor mutations [PDF]

, 1995
Male sexual differentiation and development proceed under direct control of androgens. Androgen action is mediated by the intracellular androgen receptor, which belongs to the superfamily of ligand-dependent transcription factors.
Boehmer, A.L.M. (Annemie), Brinkmann, A.O. (Albert), Brüggenwirth, H.T. (Hennie), Jenster, G.W. (Guido), Korput, J.A.G.M. (J. A G M) van der, Ris-Stalpers, C. (Carolyn), Trapman, J. (Jan)   +6 more
core   +1 more source