<?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>2026-04-26T15:53:38Z</responseDate><request verb="GetRecord" identifier="oai:repository.urosario.edu.co:10336/22420" metadataPrefix="dim">https://repository.urosario.edu.co/oai/request</request><GetRecord><record><header><identifier>oai:repository.urosario.edu.co:10336/22420</identifier><datestamp>2022-05-02T07:37:14Z</datestamp><setSpec>com_10336_39998</setSpec><setSpec>com_10336_563</setSpec><setSpec>col_10336_683</setSpec></header><metadata><dim:dim xmlns:dim="http://www.dspace.org/xmlns/dspace/dim" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.dspace.org/xmlns/dspace/dim http://www.dspace.org/schema/dim.xsd">
   <dim:field mdschema="dc" element="creator" lang="spa" authority="5cefaa73-bf47-459e-8329-b62bb42af834" confidence="-1">Malagón V.</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="accessioned">2020-05-25T23:56:25Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="available">2020-05-25T23:56:25Z</dim:field>
   <dim:field mdschema="dc" element="date" qualifier="created" lang="spa">2001</dim:field>
   <dim:field mdschema="dc" element="description" qualifier="abstract" lang="eng">In approximately 25% of patients with hereditary multiple exostosis, there is an abnormal osteochondral formation localized in the femoral proximal metaphysis. This formation often causes a mechanically progressive insufficiency of the acetabular cavity, a true developmental hip dysplasia, that together with a coxa valga deformity, which is also present, causes a gradual deterioration in the relations of this joint. This malformation has a poor prognosis and is difficult to manage. Although this entity is rather frequent and quite severe, it is rarely found in the medical literature. The author describes six private cases, taken from a total of 24,000 patients (0.25/1000) as examples of this entity, and provides a review of the literature.</dim:field>
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   <dim:field mdschema="dc" element="identifier" qualifier="doi">https://doi.org/10.1097/01241398-200103000-00014</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="issn">15392570</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="issn">02716798</dim:field>
   <dim:field mdschema="dc" element="identifier" qualifier="uri">https://repository.urosario.edu.co/handle/10336/22420</dim:field>
   <dim:field mdschema="dc" element="language" qualifier="iso" lang="spa">eng</dim:field>
   <dim:field mdschema="dc" element="publisher" lang="spa">Lippincott Williams and Wilkins</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="citationEndPage">211</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="citationIssue">No. 2</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="citationStartPage">205</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="citationTitle">Journal of Pediatric Orthopaedics</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="citationVolume">Vol. 21</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="ispartof" lang="spa">Journal of Pediatric Orthopaedics, ISSN:15392570, 02716798, Vol.21, No.2 (2001); pp. 205-211</dim:field>
   <dim:field mdschema="dc" element="relation" qualifier="uri" lang="spa">https://www.scopus.com/inward/record.uri?eid=2-s2.0-0035119756&amp;doi=10.1097%2f01241398-200103000-00014&amp;partnerID=40&amp;md5=9b54328135faede1ca1025beef0774fc</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="accesRights">info:eu-repo/semantics/openAccess</dim:field>
   <dim:field mdschema="dc" element="rights" qualifier="acceso" lang="spa">Abierto (Texto Completo)</dim:field>
   <dim:field mdschema="dc" element="source" qualifier="instname" lang="spa">instname:Universidad del Rosario</dim:field>
   <dim:field mdschema="dc" element="source" qualifier="reponame" lang="spa">reponame:Repositorio Institucional EdocUR</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Article</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Cancer surgery</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Child</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Chondroma</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Clinical article</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Female</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Genetic counseling</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Hereditary multiple exostosis</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Hip disease</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Hip dysplasia</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Human</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Hyperostosis</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Male</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Osteochondroma</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Priority journal</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Coxa valga</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Developmental dysplasia</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Ext gene family</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Femur-hip osteochondroma</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Hereditary multiple exostosis</dim:field>
   <dim:field mdschema="dc" element="subject" qualifier="keyword" lang="spa">Hip</dim:field>
   <dim:field mdschema="dc" element="title" lang="spa">Development of hip dysplasia in hereditary multiple exostosis</dim:field>
   <dim:field mdschema="dc" element="type" lang="eng">article</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="hasVersion">info:eu-repo/semantics/publishedVersion</dim:field>
   <dim:field mdschema="dc" element="type" qualifier="spa" lang="spa">Artículo</dim:field>
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