<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>45(1)</volume><submitter>Farhud DD</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Androgen insensitivity syndrome (AIS) or testicular feminization is a partial or complete inability of cell response to androgen. The cause is enzymatic defect in synthesis of testosterone, resulting sexually immature phenotypically female, with primary amenorrhea. There are three categories of AIS, complete, partial and mild, depending on the degree of external genital masculinization. The aim of this study was to find out chromosomal abnormalities, and correlation between AIS and maternal/paternal age, parents' consanguineous marriage, family history and clinical observation, in Iranian AIS patients.&lt;h4>Method&lt;/h4>This study includes a retrospective data analysis of 72,000 families' medical records in the Genetic Clinic in Tehran, during a 30-yr period (1984-2014). The</pubmed_abstract><journal>Iranian journal of public health</journal><pagination>1-5</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4822377</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Testicular Feminization or Androgen Insensitivity Syndrome (AIS) in Iran: a Retrospective Analysis of 30-Year Data.</pubmed_title><pmcid>PMC4822377</pmcid><pubmed_authors>Farhud DD</pubmed_authors><pubmed_authors>Zarif Yeganeh M</pubmed_authors><pubmed_authors>Sadighi H</pubmed_authors><pubmed_authors>Zandvakili S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Testicular Feminization or Androgen Insensitivity Syndrome (AIS) in Iran: a Retrospective Analysis of 30-Year Data.</name><description>&lt;h4>Background&lt;/h4>Androgen insensitivity syndrome (AIS) or testicular feminization is a partial or complete inability of cell response to androgen. The cause is enzymatic defect in synthesis of testosterone, resulting sexually immature phenotypically female, with primary amenorrhea. There are three categories of AIS, complete, partial and mild, depending on the degree of external genital masculinization. The aim of this study was to find out chromosomal abnormalities, and correlation between AIS and maternal/paternal age, parents' consanguineous marriage, family history and clinical observation, in Iranian AIS patients.&lt;h4>Method&lt;/h4>This study includes a retrospective data analysis of 72,000 families' medical records in the Genetic Clinic in Tehran, during a 30-yr period (1984-2014). The</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jan</publication><modification>2025-04-04T12:39:20.346Z</modification><creation>2019-06-06T15:40:34Z</creation></dates><accession>S-EPMC4822377</accession><cross_references><pubmed>27057514</pubmed></cross_references></HashMap>