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Santander" "etiqueta" => "<span class="elsevierStyleSup">g</span>" "identificador" => "aff0035" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "**" "correspondencia" => "Correspondencia: Prof. M. de Oya. Unidad de Lípidos. Fundación Jiménez Díaz. Avda. Reyes Católicos 2. 280040 Madrid." ] ] ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Clinical manifestations of heterozygous familial hipercholesterolaemia in Spain. Report of 301 cases from the central and northern areas" ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "1999-11-02" "fechaAceptado" => "1999-11-12" "PalabrasClave" => array:1 [ "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec221134" "palabras" => array:2 [ 0 => "Hipercolesterolemia familiar heterozigota" 1 => "Xantomas" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "es" => array:1 [ "resumen" => "<span class="elsevierStyleSectionTitle">Fundamento</span><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Caracterizar las manifestacionesclínicas de la hipercolesterolemia familiar(HF) en España</p> <span class="elsevierStyleSectionTitle">Pacientes y métodos</span><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Serie de 301 casos conHF procedentes del centro y norte de España.</p> <span class="elsevierStyleSectionTitle">Resultados</span><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Con un colesterol medio (DE)de 346 (58) mg/dl sólo el 7,6% de los casospresenta xantomas y el 20% cardiopatíaisquémica (CI). En el 51% existe el antecedentefamiliar de CI.</p> <span class="elsevierStyleSectionTitle">Conclusiones</span><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">En desacuerdo con la bibliografíainternacional, los xantomas son muyinfrecuentes en la HF en España, por lo quela sospecha del diagnóstico debe basarse enotras manifestaciones. La elevada presenciadel antecedente familiar de CI convierteeste aspecto en un marcador útil para eldiagnóstico y la prevención.</p>" ] "en" => array:1 [ "resumen" => "<span class="elsevierStyleSectionTitle">Rationale</span><p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">To characterize clinical manifestationsof familial hypercholesterolemia(FH) in Spain.</p> <span class="elsevierStyleSectionTitle">Patients and methods</span><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">A group of 301 cases ofFH from central and north regions of Spain.RESULTS: With a mean (SD) colesterol levelof 346 (58) mg/dl, only 7.6% of the patientshave xanthomas and 20% ischaemicheart disease. 51% have a familial historyof ischaemic heart disease.</p> <span class="elsevierStyleSectionTitle">Conclusions</span><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Different from the results of literature,xanthomas are very infrequent inFH in Spain, so diagnosis should be suspectedfrom other data. 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Manifestaciones clínicas de la hipercolesterolemia familiar heterozigota en España. Estudio de 301 casos de la zona centro y norte
Clinical manifestations of heterozygous familial hipercholesterolaemia in Spain. Report of 301 cases from the central and northern areas
Carmen Garcésa, Fernando Rodríguez Artalejob, Adalberto Serranoc, José González Bonillod, Fatima Almagroe, Juan Antonio Garridof, Manuel Zúñigag, Manuel de Oyaa,**
Autor para correspondencia
moya@fjd.es
Correspondencia: Prof. M. de Oya. Unidad de Lípidos. Fundación Jiménez Díaz. Avda. Reyes Católicos 2. 280040 Madrid.
Correspondencia: Prof. M. de Oya. Unidad de Lípidos. Fundación Jiménez Díaz. Avda. Reyes Católicos 2. 280040 Madrid.
a Unidad de Lípidos Fundación Jiménez Díaz. Madrid
b Departamento de Medicina y Salud Publica. Universidad del País Vasco
c Centro de Salud. Portugalete. Vizcaya
d Centro Salud Santo Grial. Huesca
e Hospital de Guipúzcoa. San Sebastián
f Hospital Arquitecto Marcide. El Ferrol
g Hospital Marqués de Valdecilla. Santander