Publication:
Síndromes muy poco frecuentes

dc.contributor.authorMendioroz, J
dc.contributor.authorBermejo-Sanchez, Eva
dc.contributor.authorMartínez Santana, S
dc.contributor.authorSerna, E de la
dc.contributor.authorGómez-Ullate, J
dc.contributor.authorAlcaraz, M
dc.contributor.authorAyala, A
dc.contributor.authorFelix, V
dc.contributor.authorGarcía San Miguel, M
dc.contributor.authorLara, A
dc.contributor.authorSanchis, A
dc.contributor.authorVega, M
dc.contributor.authorMansilla, E
dc.contributor.authorCuevas Catalina, María Lourdes
dc.contributor.authorMartínez-Frías, María Luisa
dc.date.accessioned2022-04-18T11:16:21Z
dc.date.available2022-04-18T11:16:21Z
dc.date.issued2005-10
dc.descriptionDismorfología, Citogenética y Clínica: Resultados de estudios sobre los datos del ECEMCes_ES
dc.description.abstractAs 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.es_ES
dc.description.peerreviewedNoes_ES
dc.format.number4es_ES
dc.format.page36-39es_ES
dc.format.volumeVes_ES
dc.identifier.citationBoletín del ECEMC: Rev Dismor Epidemiol 2005; V (nº 4): 36-39es_ES
dc.identifier.issn0210–3893es_ES
dc.identifier.journalBoletín del ECEMC: Revista de Dismorfología y Epidemiologíaes_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/14002
dc.language.isospaes_ES
dc.publisherInstituto de Salud Carlos III (ISCIII). Instituto de Investigación de Enfermedades Raras (IIER)
dc.repisalud.centroISCIII::Instituto de Investigación de Enfermedades Raras (IIER)es_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectSíndrome de macrocefalia-cutis marmorata telangiectásicaes_ES
dc.subjectSíndrome de Van der Woudees_ES
dc.subjectSíndrome de Hay-Wellses_ES
dc.subjectSíndrome de Zellwegeres_ES
dc.subjectSíndrome de Jeunees_ES
dc.subjectSíndrome de Laurin-Sandrowes_ES
dc.titleSíndromes muy poco frecuenteses_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery5764d316-caf4-47a6-b03f-4cfdc5b2e892
relation.isPublisherOfPublication13391f4b-b95b-422e-8d68-185598961e13
relation.isPublisherOfPublication.latestForDiscovery13391f4b-b95b-422e-8d68-185598961e13

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