Results 81 to 90 of about 89,384 (157)

Surface Rendering of External Genitalia of a Fetus at the 32nd Week of Gestation Affected by Partial Androgen Insensitivity Syndrome

Case Reports in Obstetrics and Gynecology, 2013
Objectives. To demonstrate the feasibility of the prenatal diagnosis of partial androgen insensitivity syndrome by 3D-4D ultrasound. Methods. To report prenatal diagnosis of partial androgen insensitivity syndrome at 32nd week of gestation by 3D-4D ...
Vincenzo Mazza, Emma Bertucci, Silvia Latella, Carlotta Cani, Pierluca Ceccarelli, Lorenzo Iughetti, Fulvia Baldinotti, Antonio Percesepe   +7 more
doaj   +1 more source

Late diagnosis of complete androgen insensitivity syndrome and transmission/carriers of the condition in a family with mutation c.2495G> T p.(Arg832Leu) in exon 7 of the androgen receptor gene: genetic, clinical and ethical aspects

Biomedical Papers, 2019
Background: The complete androgen insensitivity syndrome (CAIS) is a rare genetic disorder causing insensitivity to androgens in a person with female phenotype and 46,XY karyotype due to a mutation in the androgen receptor gene located on chromosome X ...
Renata Pomahacova, Jana Zamboryova, Petra Paterova, Anna Krepelova, Ivan Subrt, Radka Jaklova, Petra Vohradska, Eliska Hrdonkova, Josef Sykora   +8 more
doaj   +1 more source

Complete Androgen Insensitivity Syndrome

, 2018
Objective To determine whether androgen receptors affect the fatty acid profiles of neutral and polar lipids in human meibomian gland secretions. Methods Meibomian gland secretion samples were obtained from both eyes of (1) women with complete ...
Dana, Reza, Sullivan, Benjamin, Evans, James E., Cermack, Jennifer M., Sullivan, David   +4 more
core   +1 more source

Bad expression influences time to androgen escape in prostate cancer [PDF]

, 2007
<b>OBJECTIVE</b>: To assess the role of selected downstream Bcl-2 family members (Bad, Bax, Bcl-2 and Bcl-xL) in the development of androgen-independent prostate cancer (AIPC), as androgen-deprivation therapy is the treatment of choice in ...
Teo, K., Traynor, P., Mukherjee, R., Edwards, J., Gemmell, L.   +4 more
core   +1 more source

Testicular development in mice lacking receptors for follicle stimulating hormone and androgen [PDF]

, 2012
Post-natal testicular development is dependent on gonadotrophin and androgen stimulation. Follicle stimulating hormone (FSH) acts through receptors (FSHR) on the Sertoli cell to stimulate spermatogenesis while androgens promote testis growth through ...
Abel, M., Ana Monteiro, Abel Margaret, Margaret Abel, Peter J. O’Shaughnessy (171628), O’Shaughnessy Peter J., Monteiro, A., O'Shaughnessy, P.J., Ana Monteiro (171632), Peter J O'Shaughnessy, Margaret Abel (171636), Monteiro Ana   +11 more
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Androgen insensitivity

, 1998
Adapted with permission from Jaffe R.B. Disorders of Sexual Differentiation. In Yen SSC and Jaffe RB, eds, Reproductive Endocrinology, W.B. Saunders Co., Philadelphia, 1986, p 300.
Peterson, C. Matthew
core  

Phenotypic diversity in siblings with partial androgen insensitivity syndrome

, 1997
The androgen insensitivity syndrome is a heterogeneous disorder with a wide spec-trum of phenotypic abnormalities, rang-ing from complete female to ambiguous forms that more closely resemble males. The primary abnormality is a defective androgen receptor
Bevan, C. L., Gregory, John Welbourn, I A Hughes, B A J Evans, M N Patterson, Patterson, M. N., J W Gregory, C L Bevan, Hughes, I. A., Evans, Bronwen Alice James   +9 more
core   +1 more source

Androgen insensitivity syndrome: do trinucleotide repeats in androgen receptor gene have any role?

, 2008
Aim: To investigate the role of CAG and GGN repeats as genetic background affecting androgen insensitivity syndrome (AIS) phenotype. Methods: We analyzed lengths of androgen receptor (AR)-CAG and GGN repeats in 69 AIS cases, along with 136 unrelated ...
Gupta, Nalini J., Chakravarty, Baidyanath, Singh, Lalji, Rajender, Singh, Thangaraj, Kumarasamy   +4 more
core   +1 more source

The Physiological, Psychological and Genetic Expressions of XY Female Reporting at Tertiary Care Infertility Clinic of Kingdom of Saudi Arabia

Pakistan Journal of Medical Research, 2022
Background: Disorder in sex development (DSD) refers to a variety of diagnoses in which the development of chromosomal make-up, gonadal development, or anatomical development is abnormal.
Munazzah Rafique, Dania Al Jaroudi
doaj  

Complete Androgen Insensitivity Syndrome in Three Sisters [PDF]

International Journal of Fertility and Sterility, 2014
Disorders of sexual development (DSD) are congenital anomalies due to atypical development of chromosomes, gonads and anatomy. Complete androgen insensitivity syndrome (CAIS), also known as testicular feminization (TF) is a rare DSD disease. The majority
Levent Verim
doaj