<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1135-5727</journal-id>
<journal-title><![CDATA[Revista Española de Salud Pública]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Esp. Salud Publica]]></abbrev-journal-title>
<issn>1135-5727</issn>
<publisher>
<publisher-name><![CDATA[Ministerio de Sanidad]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1135-57272021000100192</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Cribado neonatal del hipotiroidismo congénito]]></article-title>
<article-title xml:lang="en"><![CDATA[Neonatal screening for congenital hypothyroidism]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[López-Galera]]></surname>
<given-names><![CDATA[Rosa Mª]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Castiñeiras-Ramos]]></surname>
<given-names><![CDATA[Daisy]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rocha]]></surname>
<given-names><![CDATA[Hugo]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
<xref ref-type="aff" rid="Aaf"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Hospital Clínic de Barcelona Servicio de Bioquímica y Genética Molecular Laboratorio de Cribado Neonatal. Sección de Errores Congénitos del Metabolismo]]></institution>
<addr-line><![CDATA[Barcelona ]]></addr-line>
<country>España</country>
</aff>
<aff id="Af2">
<institution><![CDATA[,Hospital Clínico Universitario de Santiago de Compostela Laboratorio de Metabolopatías ]]></institution>
<addr-line><![CDATA[Santiago de Compostela A Coruña]]></addr-line>
<country>España</country>
</aff>
<aff id="Af3">
<institution><![CDATA[,Instituto Nacional de Saúde Doutor Ricardo Jorge de Oporto Human Genetics Department Newborn Screening, Metabolism and Genetics Unit]]></institution>
<addr-line><![CDATA[Oporto ]]></addr-line>
<country>Portugal</country>
</aff>
<aff id="Af4">
<institution><![CDATA[,Sociedad Española de Medicina del Laboratorio Comisión de Diagnóstico Perinatal ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
<country>España</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>00</month>
<year>2021</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>00</month>
<year>2021</year>
</pub-date>
<volume>95</volume>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_arttext&amp;pid=S1135-57272021000100192&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_abstract&amp;pid=S1135-57272021000100192&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.isciii.es/scielo.php?script=sci_pdf&amp;pid=S1135-57272021000100192&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[RESUMEN  Fundamentos: Las hormonas tiroideas son fundamentales para un desarrollo cerebral normal, siendo el hipotiroidismo congénito (HC) la causa más frecuente de retraso mental que se puede prevenir. La detección precoz del HC es de interés primordial en Salud Pública y Medicina Preventiva y está incluida en los programas de cribado neonatal. En los recién nacidos detectados y que inician tratamiento en los primeros días de vida se consigue reducir la morbilidad, mortalidad y las posibles discapacidades asociadas a la enfermedad. El objetivo de la revisión fue poner de manifiesto la relevancia que tienen los programas de detección del HC, conocer la situación actual a nivel nacional y mundial y los desafíos y perspectivas de futuro.  Métodos: La revisión se ha basado en la selección de estudios y revisiones de la enfermedad y de estudios publicados de diferentes programas de cribado para la detección del HC. Como fuentes de información se han utilizado bases de referencias bibliográficas, guías y/o protocolos de sociedades científicas, documentos de agencias tecnológicas evaluadoras y documentos de organismos oficiales.  Resultados: En todas las referencias consultadas se ha podido constatar en función de los casos detectados, valor predictivo positivo y prevalencias que la detección precoz del HC ha resultado de una gran eficiencia para el diagnóstico de la enfermedad.  Conclusiones: El cribado neonatal del HC primario es un ejemplo de éxito en salud pública. Son necesarias líneas de investigación para aclarar si otras formas moderadas del HC se benefician de su detección y tratamiento precoz.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[ABSTRACT  Background: Thyroid hormones are essential for normal brain development, with congenital hypothyroidism (CH) being the most frequent cause of mental retardation that can be prevented. The early detection of CH is of primary interest in Public Health and Preventive Medicine and is included in neonatal screening programs. In newborns detected and starting treatment in the first days of life, morbidity, mortality and possible disabilities associated with the disease are reduced. The objective of the review was to highlight the relevance of HC detection programs, to know the current situation at the national and global level and the challenges and future prospects.  Methods: The review was based on the selection of studies and reviews of the disease and published studies of different screening programs for the detection of CH. As sources of information, bibliographic reference bases, guides and / or protocols of scientific societies, documents of technological evaluation agencies and documents of official organizations have been used.  Results: In all the references consulted, it has been possible to verify based on the cases detected, positive predictive value and prevalences that the early detection of CH has been highly efficient for the diagnosis of the disease.  Conclusions: Neonatal screening for primary CH is an example of success in public health. Lines of research are needed to clarify whether other moderate forms of CH benefit from early detection and treatment.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Hormonas tiroideas]]></kwd>
<kwd lng="es"><![CDATA[Morbilidad]]></kwd>
<kwd lng="es"><![CDATA[Hipotiroidismo congénito]]></kwd>
<kwd lng="es"><![CDATA[Cribado neonatal]]></kwd>
<kwd lng="es"><![CDATA[Estrategias de determinación de hipotiroidismo congénito]]></kwd>
<kwd lng="es"><![CDATA[Bases de datos bibliográficos]]></kwd>
<kwd lng="en"><![CDATA[Thyroid hormones]]></kwd>
<kwd lng="en"><![CDATA[Morbidity]]></kwd>
<kwd lng="en"><![CDATA[Congenital hypothyroidism]]></kwd>
<kwd lng="en"><![CDATA[Neonatal screening]]></kwd>
<kwd lng="en"><![CDATA[Strategies for determining congenital hypothyroidism]]></kwd>
<kwd lng="en"><![CDATA[Bibliographic databases]]></kwd>
</kwd-group>
</article-meta>
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