<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-05T14:30:05Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/14002" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/14002</identifier><datestamp>2025-03-13T08:35:31Z</datestamp><setSpec>com_20.500.12105_5571</setSpec><setSpec>com_20.500.12105_2404</setSpec><setSpec>com_20.500.12105_2403</setSpec><setSpec>col_20.500.12105_5614</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Mendioroz, J</subfield>
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      <subfield code="a">Bermejo-Sanchez, Eva</subfield>
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      <subfield code="a">Martínez Santana, S</subfield>
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      <subfield code="a">Serna, E de la</subfield>
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      <subfield code="a">Gómez-Ullate, J</subfield>
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      <subfield code="a">Alcaraz, M</subfield>
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      <subfield code="a">Felix, V</subfield>
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      <subfield code="a">García San Miguel, M</subfield>
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      <subfield code="a">Lara, A</subfield>
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      <subfield code="a">Vega, M</subfield>
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      <subfield code="a">Mansilla, E</subfield>
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      <subfield code="a">Cuevas Catalina, María Lourdes</subfield>
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      <subfield code="a">Martínez-Frías, María Luisa</subfield>
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      <subfield code="c">2005-10</subfield>
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      <subfield code="a">As in previous years, six new syndromes have been selected to be included in this section, aimed to make easier the recognition of syndromes with low-frequency by paediatricians and first health care physicians, particularly those of rural areas. In this Boletín, the following syndromes are included: Megalencephaly-Cutis Marmorata Telangiectatica Congenita syndrome, Van der Woude syndrome, Hay Wells syndrome, Zellweger syndrome, Jeune syndrome and Laurin-Sandrow syndrome. For each syndrome, the most important clinical characteristics, and the present knowledge on their causal factors and mechanisms involved are sumarized.</subfield>
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      <subfield code="a">Boletín del ECEMC: Rev Dismor Epidemiol 2005; V (nº 4): 36-39</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/14002</subfield>
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      <subfield code="a">Síndrome de macrocefalia-cutis marmorata telangiectásica</subfield>
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      <subfield code="a">Síndrome de Van der Woude</subfield>
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      <subfield code="a">Síndrome de Hay-Wells</subfield>
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      <subfield code="a">Síndrome de Zellweger</subfield>
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      <subfield code="a">Síndrome de Jeune</subfield>
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      <subfield code="a">Síndromes muy poco frecuentes</subfield>
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