<?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>2026-05-17T00:18:32Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/26809" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/26809</identifier><datestamp>2025-12-18T13:01:55Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</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">David, Sánchez-Ortiz</subfield>
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      <subfield code="a">Lucía, Deiros-Bronte</subfield>
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      <subfield code="a">Lucía, De la Hoz-Marañón</subfield>
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      <subfield code="a">Marta, Feito-Rodríguez</subfield>
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      <subfield code="a">Juvenal, Rey-Lois</subfield>
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      <subfield code="a">Diana, Salas-Mera</subfield>
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      <subfield code="a">Carlos, Labrandero-De Lera</subfield>
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      <subfield code="a">Juan Carlos, López-Gutiérrez</subfield>
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      <subfield code="a">Federico, Gutiérrez-Larraya</subfield>
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      <subfield code="a">PHACE syndrome is an uncommon disorder, marked by large segmental hemangiomas on the face and various developmental anomalies. Significant advancements have been made in its diagnosis, imaging, and understanding of complications since 1996. We describe the first diagnosis case of PHACE syndrome in a one-month and 19-day-old infant who presented with a large facial hemangioma and coarctation of the aorta originating from the left common carotid artery, along with an aberrant course of the right subclavian artery. The complementary diagnostic studies, their surgical correction, and their progression are described. Given the rarity of the syndrome (the PHACE Syndrome International Clinical Registry and Genetic Repository has over 270 enrolled individuals) and the importance of early diagnosis of some anomalies it comprises, particularly cardiovascular anomalies, dissemination is considered crucial for general and pediatric cardiologists.</subfield>
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      <subfield code="a">Front Cardiovasc Med. 2025 Feb 3:12:1539168.</subfield>
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      <subfield code="a">FRONTIERS IN CARDIOVASCULAR MEDICINE</subfield>
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      <subfield code="a">https://hdl.handle.net/20.500.12105/26809</subfield>
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      <subfield code="a">PHACE syndrome</subfield>
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      <subfield code="a">aortic coarctation</subfield>
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      <subfield code="a">Case Report: Two-month-old infant with PHACE syndrome: facial hemangioma and severe complex coarctation of the aorta.</subfield>
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