Androgen insensitivity syndrome is due to hormone resistance which may be due to defective androgen receptor (AR) function by either abnormal androgen receptor (AR) binding, decreased receptor binding, or impaired androgen receptor (AR) binding. AIS is an X linked disorder. The development of androgen insensitivity syndrome is a result of genetic mutations of the androgen receptor (AR) gene located on the chromosome Xq11-12. Associated conditions include primary amenorrhea, infertility and dyspareunia.

• Androgen resistance may develop during fetal development and after birth.
• The hormone resistance may be due to defective androgen receptor (AR) function by either abnormal androgen receptor (AR) binding, decreased receptor binding, or impaired androgen receptor (AR) binding. ^[1][2][3]
• A spectrum of phenotypes may be caused due to missense mutations in the androgen receptor (AR) protein. The two important domains of the receptor protein namely DBD and LDB domains are the ones wherein the most frequent missense mutations are found.^[4][5]
• The phenotypic variability impacts and translates the degree to which ligand-binding and receptor functions are disrupted by different substitutions.^[4][6]
• The genetic background has an influence on the resulting phenotype as a result of the same mutation which may lead to different forms of AIS within a family.^[4][7]
• Mutations in the androgen receptor (AR) gene helps as a trusted tool for the diagnosis and molecular subclassification of AIS. The resulting phenotype is affected by the kind of amino acid substitution occurring due to mutation.^[4]
• Information regarding the mutation in the androgen receptor (AR) and its functional consequences helps in determining the genotype-phenotype correlation, to improve and better manage the cases of male pseudohermaphroditism pertaining to surgery of the genitalia, gonadectomy and gender assignment. ^[4]
• The lack of virilization of external genitalia is due to the failure of genital folds to fuse and to form scrotum and penis.
• The agenesis of the fallopian tubes, uterus, cervix and proximal vagina is due to the simultaneous testicular production of mullerian inhibiting factor which regresses the mullerian structures.
• In CAIS (complete androgen insensitivity syndrome), the development of the wolffian duct and the differentiation of male external genitalia do not occur correctly, and the Mullerian ducts regress due to the presence of anti-Mullerian hormone (AMH) produced by the sertoli cells of normally developed gonads. The residual Mullerian structures exist in approximately one third of patients. ^{[8] [9]}
• The female phenotype along with breast development is a result of the peripheral aromatization of testosterone into estrogen.^[10]
• As a result of the defective androgen receptor (AR) due to imperfect feedback mechanism of testosterone at the pituitary and hypothalamus there are elevated levels of serum testosterone, FSH and LH observed.
• Testosterone biosynthetic defects are ruled out by the normal serum 17α hydroxyprogesterone, DHEA and androstenedione levels.^[11]
• Sufficient peripheral conversion of testosterone is indicative of normal estradiol level.

• AIS is an X linked disorder. ^[12]
• A high proportion of De novo mutations arise after the zygote stage which occur at a high rate within the androgen receptor (AR) gene.^[12]
• Spontaneous mutations in the androgen receptor (AR) gene results in androgen insensitivity syndrome even without any family history.^[12]
• The development of androgen insensitivity syndrome is a result of genetic mutations of the androgen receptor (AR) gene located on the chromosome Xq11-12.^[4][12]
• Different mutations in the androgen receptor (AR) gene leads to varied clinical phenotypes.^[13][14]
• There have been more than 800 mutations in the androgen receptor (AR) gene reported in AIS patients. ^[15]

• Primary amenorrhea
• Infertility
• Dyspareunia
• Common testicular tumors seen in the Androgen insensitivity syndrome are: ^[16]

• Germ cell tumors
• Sex cord tumors (seminoma)
• Sertoli cell tumors
• Leydig cell tumors
• Hamartomas

• Complete androgen insensitivity syndrome in a 30 years old woman presenting with primary amenorrhea.^[17]. ^[18]

• 
  Front and side view of the patient by Regragui Souhail et al from The Pan African Medical Journal – ISSN 1937-8688. Pan Afr Med J. 2016;25:199. Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0). ^[17]
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  Clinical aspect of the vagina by Regragui Souhail et al from The Pan African Medical Journal – ISSN 1937-8688. Pan Afr Med J. 2016;25:199. Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0). ^[17]
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  Intra- abdominal testes – Laparoscopic aspect by Regragui Souhail et al from The Pan African Medical Journal – ISSN 1937-8688. Pan Afr Med J. 2016;25:199. Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0). ^[17]
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  The excised testis – Macroscopic aspect by Regragui Souhail et al from The Pan African Medical Journal – ISSN 1937-8688. Pan Afr Med J. 2016;25:199. Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0). ^[17]

• Histopathology of testes shows atrophic seminiferous tubules containing only sertoli cells, associated to a leydig cells hyperplasia.^[18]
• The well-limited nodule presents as a circumscribed structure with a thin capsule consisting of atrophic servolian tubes with a very small interstitial tissue with rare leydig cells. This nodule corresponds to a well differentiated tumor with sertoli-leydig cells. ^[17]
• The gonads on histopathological examination show the following: ^[16]

• Thickened tunica albuginea
• Seminiferous tubules with primary and secondary spermatogonia and sertoli cells
• Intertubular leydig cells were seen along with peritubular fibrosis

• 
  Testes – Atrophy of the seminiferous tubules – Histopathological aspect, HE staining by Regragui Souhail et al from The Pan African Medical Journal – ISSN 1937-8688. Pan Afr Med J. 2016;25:199. Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0). ^[17]
• 
  Testicular parenchyma of lobulated architecture, made of seminiferous tubes of atrophic appearance; these tubes are lined with Sertolia cells, with no obvious signs of spermatogenesis the interstitium is fibrous with rare clusters of Leydig cells by Boutaina Lachiri et al from the Pan African Medical Journal – ISSN 1937-8688. Pan Afr Med J. 2015;20:400. CC BY-NC 3.0, Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/3.0). ^[18]