Publication:
Síndromes muy poco frecuentes

dc.contributor.authorMartínez-Frías, María Luisa
dc.contributor.authorMendioroz, J
dc.contributor.authorLópez Grondona, Fermín
dc.contributor.authorBermejo-Sanchez, Eva
dc.contributor.authorRodríguez-Pinilla, Elvira
dc.contributor.authorAparicio, P
dc.contributor.authorBlanco, M
dc.contributor.authorCuevas Catalina, María Lourdes
dc.contributor.authorFoguet, A.
dc.contributor.authorLópez, JA
dc.contributor.authorPlaja, P
dc.contributor.authorPantoja, A
dc.contributor.authorRodriguez, Laura
dc.contributor.authorRodríguez, A
dc.contributor.authorValdivia, L
dc.contributor.authorVázquez MS
dc.date.accessioned2022-02-17T09:50:14Z
dc.date.available2022-02-17T09:50:14Z
dc.date.issued2003-10
dc.descriptionDismorfología, Citogenética y Clínica: Resultados sobre los datos del ECEMCes_ES
dc.description.abstractThis section is based on two facts: First, that the majority of the malformation syndromes are very few frequent. Second, the progressive generalization in our country of the prenatal diagnosis with a high resolution echography performed to all women between 18-20 weeks of gestation as a Service of the National Health System, together with the possibility of voluntary interruption of gestation if fetal anomalies are detected. Thus, the impact of prenatal diagnosis is that the frequency at birth of these syndromes shows an important and progressive decreasing trend. For these reasons, in addition to the difficulty for pediatricians and geneticists or our population to diagnose these usually rare syndromes, the impact of prenatal diagnosis increases the usual difficulties that the young pediatricians and geneticists have to identify these pathologies. This increases the possibility that some affected patients can remain undiagnosed for a long time, or even never be diagnosed. As started last year in this section of the "Boletín del ECEMC", we present other six syndromes of low frequency in our country.es_ES
dc.description.peerreviewedNoes_ES
dc.format.number2es_ES
dc.format.page30-33es_ES
dc.format.volumeVes_ES
dc.identifier.citationBoletín del ECEMC: Rev Dismor Epidemiol 2003; V (nº 2): 30-33es_ES
dc.identifier.issn0210-3893es_ES
dc.identifier.journalBoletín del ECEMC: Revista de Dismorfología y Epidemiologíaes_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/13661
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.subjectDismorfologíaes_ES
dc.subjectAnomalías congénitases_ES
dc.subjectEpidemiologíaes_ES
dc.subjectSíndrome de Robinow recesivoes_ES
dc.subjectSíndrome de Goltzes_ES
dc.subjectSíndrome de Greiges_ES
dc.subjectSíndrome de Oto-Palato-Digitales_ES
dc.subjectSíndrome de Kingstones_ES
dc.subjectSíndrome de Displasia metatropicaes_ES
dc.titleSíndromes muy poco frecuenteses_ES
dc.title.alternativeVery few frequent syndromeses_ES
dc.typeresearch articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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