Results 191 to 200 of about 28,940 (212)
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Testicular feminization syndrome (Androgen insensitivity)
Journal of Pediatric Surgery, 1981Three children with testicular feminization syndrome have been seen in the past 4 yr. Each presented with at least one large inguinal hernia. The gonad was proven to be a testis by frozen section. Gonadectomy and herniorrhaphy were done. The plan is to remove the second gonad after puberty.
D G, Marshall, G H, Valentine
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Androgen insensitivity syndrome: Can cytology help?
Cytopathology, 2021Androgen insensitivity syndrome (AIS) is described as a patient's clinical (phenotypical) presentation as a female with male karyotyping. Classically, patients are normal looking females with complaints of primary amenorrhea.
Sakshi Dahiya +5 more
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Androgen insensitivity syndrome
Reproductive Medicine Review, 1992Over the past four years, major advances in the understanding of the aetiology and pathogenesis of the androgen insensitivity syndrome (AIS) have occurred. This review aims to summarize current information on clinical, diagnostic, therapeutic and molecular aspects of AIS.
Jennifer A Batch +2 more
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Human Androgen Insensitivity Syndrome
Journal of Andrology, 1995The clinical and pathophysiologic features of AIS provide a human model for understanding the role of androgen and its receptor in the induction and maintenance of male sex differentiation and function. Upon inspection, one is immediately impressed by the diverse nature of the mutations involved in the spectrum of AIS and the heterogeneous distribution
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Induced Lactation in a Mother Through Surrogacy With Complete Androgen Insensitivity Syndrome (CAIS)
Journal of Human Lactation, 2020Introduction Breastfeeding offers the optimal feeding option for newborns in terms of nutritional content and reinforces mother-infant bonding. As a physiological process intrinsically linked to parturition, breastfeeding is no longer reserved for ...
M. LeCain, G. Fraterrigo, W. Drake
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Androgen insensitivity syndrome: a review
Journal of Endocrinological Investigation, 2023E. Delli Paoli +5 more
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Journal of investigative surgery, 2019
Background: Complete androgen insensitivity syndrome (CAIS) is a congenital condition caused by genetic defects in the androgen receptor (AR) gene located on the X chromosome, which lead to a phenotypical female individual with a 46, XY karyotype.
N. Listyasari +8 more
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Background: Complete androgen insensitivity syndrome (CAIS) is a congenital condition caused by genetic defects in the androgen receptor (AR) gene located on the X chromosome, which lead to a phenotypical female individual with a 46, XY karyotype.
N. Listyasari +8 more
semanticscholar +1 more source
[Androgen insensitivity syndromes].
Annales d'urologie, 1987The syndromes of androgen resistance illustrate a special field of endocrinology, that is pathology of target-tissues. These syndromes are responsible for male pseudohermaphroditism and provoke in XY subjects, with a normal testicular androgen secretion, abnormalities in the phenotype with all the possibilities from an "idealistically" female phenotype
F, Kuttenn +4 more
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