androgen insensitivity syndrome

(redirected from Complete androgen insensitivity)
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androgen insensitivity syndrome

[¦an·drə·jən in‚sen·sə′tiv·ə·dē ‚sin‚drōm]
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Most of 46 XX CAH patients, even if markedly virilised, and 46 XY complete androgen insensitivity syndrome are raised as females.26,27 Surgery include clitorplasty, labioplasty and vaginoplasty28 but almost 90% will only require vaginoplasty.29 Patients of 5-[alpha] reductase deficiency30 and 17-[beta] hydroxysteroid dehydrogenase deficiency31 are assigned to the male gender.
Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor gene.
Complete Androgen Insensitivity Syndrome Caused by a Novel Mutation in the Ligand-Binding Domain of the Androgen Receptor: Functional Characterization.
Results: Out of 151 patients of XY DSD, 68 (45%) patients were diagnosed as partial androgen insensitivity syndrome (PIAS), 18 (12%) as isolated micropenis, 25 (16.6%) as partial gonadal dysgenesis, 12 (7.9%) as hypogonadotropic hypogonadism, 11 (7.2%) as primary hypogonadism, 13 (8.6%) as complete androgen insensitivity syndrome (CAIS) and 4 (2.6%) as 5[alpha] reductase deficiency.
(2) Swyer syndrome should be included in the differential diagnosis of complete androgen insensitivity syndrome (CAIS) and 17a-hydroxylase deficiency syndrome, which also present with a 46XY karyotype.
(14) Increased signs and symptoms of dry eye and MGD have been found in patients on antiandrogens (such as in prostate or breast cancer treatment) and in women with complete androgen insensitivity syndrome (CAIS).
Conway, "Comparison of bone mineral density and body proportions between women with complete androgen insensitivity syndrome and women with gonadal dysgenesis," European Journal of Endocrinology, vol.
Is complete androgen insensitivity syndrome associated with alterations in the meibomian gland and ocular surface?
Patraccom et al., "Testicular feminization: complete androgen insensitivity syndrome.
Hence, a diagnosis of complete androgen insensitivity syndrome with germ cell tumor with retroperitoneal lymph node metastasis was made.
46XY individuals with complete androgen insensitivity syndrome (CAIS) lack a functioning androgen receptor, and their tissues are unable to respond to testosterone/DHT.
Patients with complete androgen insensitivity syndrome were advised female gender.

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