Partial Androgen Insensitivity Syndrome
What's New
Last Posted: May 25, 2024
- Clinical, Hormonal, and Genetic Spectrum of 46 XY Disorders of Sexual Development (DSD) Patients.
Rajan Palui, et al. Indian journal of pediatrics 2024 0 - Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor.
Batista Rafael Loch, et al. Journal of pediatric endocrinology & metabolism : JPEM 2017 0 (2) 223-228 - Clinical characteristics, AR gene variants, and functional domains in 64 patients with androgen insensitivity syndrome.
Liu Q, et al. Journal of endocrinological investigation 2022 0 (1) 151-158 - Screening for mutations in 17ß-hydroxysteroid dehydrogenase and androgen receptor in women presenting with partially virilised 46,XY disorders of sex development.
Phelan Niamh, et al. European journal of endocrinology / European Federation of Endocrine Societies 2015 3 - Low frequency of androgen receptor gene mutations in 46 XY DSD, and fetal growth restriction.
Lek Ngee, et al. Archives of disease in childhood 2014 4 (4) 358-61 - Minor hypospadias: the "tip of the iceberg" of the partial androgen insensitivity syndrome.
Kalfa Nicolas, et al. PloS one 2013 0 (4) e61824 - Partial androgen insensitivity syndrome
From NCATS Genetic and Rare Diseases Information Center - Correlation between genotype, phenotype and sex of rearing in 111 patients with partial androgen insensitivity syndrome.
Deeb A, et al. Clinical endocrinology 2005 7 (1) 56-62
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- Page last reviewed:Feb 1, 2024
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