<?xml version="1.0"?>
<record>
  <id>https://homosaurus.org/v3/homoit0001079</id>
  <identifier>homoit0001079</identifier>
  <prefLabel language="en">Partial androgen insensitivity syndrome</prefLabel>
  <altLabel language="en">PAIS</altLabel>
  <issued>
    <value>2019-05-14</value>
    <name>xsd:date</name>
  </issued>
  <modified>
    <value>2021-12-08</value>
    <name>xsd:date</name>
  </modified>
  <broader>
    <id>https://homosaurus.org/v3/homoit0000044</id>
    <prefLabel language="es">S&#xED;ndrome de insensibilidad a los andr&#xF3;genos</prefLabel>
  </broader>
  <broader>
    <id>https://homosaurus.org/v3/homoit0000669</id>
    <prefLabel language="es">Variaciones intersex</prefLabel>
  </broader>
  <comment language="en">People with partial androgen insensitivity (PAIS) have some response to testosterone, but not as much as is typical for people with XY chromosomes without androgen insensitivity. People with PAIS may be born with testes that are undescended or partially descended and with genital differences such as a vaginal opening that is shallower than typical, a phallus that may be perceived as a large clitoris or a small penis, and variations affecting their urethra. They might also be born with genitals that look more like a penis or like a vulva and vagina. In adolescence, people with PAIS may develop some features that are associated with a typical testosterone puberty and others that are associated with a typical estrogen puberty since their body responds to some of the testosterone that their gonads produce while the rest is converted into estrogen.</comment>
</record>
