Results 21 to 30 of about 3,490,978 (179)

Psychological and family intervention with a person diagnosed with complete androgen insensitivity syndrome

Telangana Journal of Psychiatry, 2023
Complete androgen insensitivity syndrome (CAIS) is a rare condition resulting due to the inability of the cell to respond to the masculine hormone (androgen). Often, CAIS patients identify themselves as female and may experience significant psychological
Mysore Narasimha Vranda, Suresh Badamath, Marita Kadicheeni Paul, Radhakrishnan Vasanthra Cicil, Prakyath Ravindranath Hegde, Adharsa Ajayan, Hari Hara Suchendra, Tshering Lhamu   +7 more
doaj   +2 more sources

Integrative Transcriptomic Analysis and Preliminary Peripheral Blood Evaluation Identify <i>ASAP2</i> as an Exploratory Candidate Molecule Associated with Complete Androgen Insensitivity Syndrome. [PDF]

Int J Gen Med
Luo C, Duan C, Xu S, Xu J, Wang S, Zheng L, Yu X, He D.   +7 more
europepmc   +3 more sources

Complete androgen insensitivity syndrome as a condition requiring interdisciplinary care – A case report [PDF]

Annales Academiae Medicae Silesiensis
Complete androgen insensitivity syndrome (CAIS; also known as Morris syndrome) is a rare disorder associated with mutations in the androgen receptor gene located on the X chromosome.
Daria Rost, Julia Gniewek, Małgorzata Jekiełek, Janusz Strzelczyk   +3 more
doaj   +2 more sources

Bone density and skeletal turnover in complete androgen insensitivity syndrome. [PDF]

J Endocr Soc
Jovanovic M, Laufer A, Stein D, St Ville ME, Musaad S, Jumani S, Kaur H, Gomez-Lobo V, Gordon CM.   +8 more
europepmc   +2 more sources

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

Clin Case Rep
Francesca AM, Serena S, Chiara DB, Angela RM, Basilia P, Marco C, Mattia G, Maddalena RR, Emanuela E, Silvana B, Salvatore C.   +10 more
europepmc   +2 more sources

Complete androgen insensitivity syndrome presenting with bilateral adnexal masses and mixed gonadal histopathology. [PDF]

Arch Gynecol Obstet
Yildiz AG, Kurt A, Cengiz ID, Arslankoz S, Gultekin IB.   +4 more
europepmc   +3 more sources

Case Report: Familial complete androgen insensitivity syndrome across four sisters from childhood to adulthood - a hemizygous AR p.Trp742Leu variant and a 14-year failure to initiate familial cascade evaluation. [PDF]

Front Endocrinol (Lausanne)
Çakmak B, Gündoğan S, Tektaş D.
europepmc   +2 more sources

Complete Androgen Insensitivity Syndrome (CAIS) Genetic Counseling: Navigating Germline Mosaicism Concerns. [PDF]

Case Rep Genet
Iacono LM, Levy PA, Baer TG.
europepmc   +2 more sources

Clinical Characteristics and Management of Two Cases of Complete Androgen Insensitivity Syndrome With Germ Cell Tumors. [PDF]

Cancer Rep (Hoboken)
Wang F, Wang D, Li J, Xing N.
europepmc   +3 more sources

Expanding the Molecular Landscape of Androgen Insensitivity Syndrome Through Next-Generation Sequencing [PDF]

The Application of Clinical Genetics
Tadeusz Kałużewski,1,2 Iwona Pinkier,1 Urszula Wysocka,1 Jordan Sałamunia,2 Łukasz Kępczyński,1,2 Małgorzata Piotrowicz,1 Bogdan Kałużewski,2 Agnieszka Gach1 1Department of Genetics, Polish Mother’
Kałużewski T, Pinkier I, Wysocka U, Sałamunia J, Kępczyński Ł, Piotrowicz M, Kałużewski B, Gach A   +7 more
doaj   +1 more source