Results 21 to 30 of about 8,273 (242)

Complete androgen insensitivity syndrome: Dilemmas for further management after gonadectomy

Journal of Human Reproductive Sciences, 2019
Complete androgen insensitivity syndrome is a rare condition, wherein a genetic male is phenotypically female and is raised as a female. Treatement requires timely gonadectomy, need for long term hormonal replaceent therapy, psycological and genetic ...
Pratibha Singh, Meenakshi Gothwal, Garima Yadav, Kuldeep Singh   +3 more
doaj   +2 more sources

Serial evaluation of gonads of complete androgen insensitivity syndrome from birth to puberty: Is gonadectomy necessary? [PDF]

Urol Case Rep
Ueda Y, Matsumoto F, Matsui F, Matsuyama S.   +3 more
europepmc   +2 more sources

Dilemmas in management of osteoporosis in patients with complete androgen insensitivity syndrome. [PDF]

BMJ Case Rep, 2021
Slayden T, Bauer EM, Shakir MK, Hoang TD.   +3 more
europepmc   +3 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

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

Testicular development in the complete androgen insensitivity syndrome [PDF]

The Journal of Pathology, 2006
AbstractThe complete androgen insensitivity syndrome (CAIS), caused by mutations in the androgen receptor (AR) gene, is associated with abnormal testicular development and an increased risk of germ cell malignancy. Previous histological studies in CAIS have selected patients purely on the basis of clinical diagnosis and were mostly based on small ...
Sabine E Hannema, Ian Scott, Ewa Rajpert‐De Meyts, NE Skakkebæk, Nick Coleman, IA Hughes   +5 more
openalex   +4 more sources

COMPLETE ANDROGEN INSENSITIVITY SYNDROME [PDF]

International Journal of Advanced Research, 2016
D.G.O Dr.L.Santhanalakshmi
openalex   +2 more sources

Rare Case of Complete Androgen Insensitivity Syndrome. [PDF]

Cureus
Androgen insensitivity syndrome is a rare X-linked recessive condition in which patients present a female phenotype. After complete androgen insensitivity syndrome (CAIS) diagnosis, the timing of gonadectomy should be evaluated, considering the risks and benefits of this procedure.
Fava Spessoto LC, Avelino Silveira JS, Abularach AM, Santana Garcia G, Almeida MC, Gonzales GC, Nagle Spessoto AC, Facio FN, Silva Faria MH.   +8 more
europepmc   +3 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