<?xml version="1.0"?>
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  <leader>00596nz  a2200217n  4500</leader>
  <controlfield tag="008">230628|||anznnbab||||||||||||||a|||||||d</controlfield>
  <datafield tag="024" ind1="8" ind2=" ">
    <subfield code="a">homoit0002879</subfield>
    <subfield code="0">https://homosaurus.org/v3/homoit0002879</subfield>
  </datafield>
  <datafield tag="040" ind1=" " ind2=" ">
    <subfield code="f">homoit</subfield>
  </datafield>
  <datafield tag="150" ind1=" " ind2=" ">
    <subfield code="a">Type 1 Leydig cell hypoplasia</subfield>
  </datafield>
  <datafield tag="450" ind1=" " ind2=" ">
    <subfield code="a">Type 1 LCH</subfield>
  </datafield>
  <datafield tag="550" ind1=" " ind2=" ">
    <subfield code="a">Hipoplasia de c&#xE9;lulas de Leydig</subfield>
    <subfield code="0">https://homosaurus.org/v3/homoit0002863</subfield>
  </datafield>
  <datafield tag="680" ind1=" " ind2=" ">
    <subfield code="a">People with Type 1 Leydig cell hypoplasia (LCH) produce almost no testosterone and will usually be born with a vulva and vagina and undescended testes. They are usually assigned female at birth, often without their variation being recognized until adolescence, at which point they generally will not develop any secondary sex characteristics or experience other changes typically associated with puberty.</subfield>
  </datafield>
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