Publication: Síndromes muy poco frecuentes
| dc.contributor.author | Mendioroz, J | |
| dc.contributor.author | Bermejo-Sanchez, Eva | |
| dc.contributor.author | Martínez Santana, S | |
| dc.contributor.author | Serna, E de la | |
| dc.contributor.author | Gómez-Ullate, J | |
| dc.contributor.author | Alcaraz, M | |
| dc.contributor.author | Ayala, A | |
| dc.contributor.author | Felix, V | |
| dc.contributor.author | García San Miguel, M | |
| dc.contributor.author | Lara, A | |
| dc.contributor.author | Sanchis, A | |
| dc.contributor.author | Vega, M | |
| dc.contributor.author | Mansilla, E | |
| dc.contributor.author | Cuevas Catalina, María Lourdes | |
| dc.contributor.author | Martínez-Frías, María Luisa | |
| dc.date.accessioned | 2022-04-18T11:16:21Z | |
| dc.date.available | 2022-04-18T11:16:21Z | |
| dc.date.issued | 2005-10 | |
| dc.description | Dismorfología, Citogenética y Clínica: Resultados de estudios sobre los datos del ECEMC | es_ES |
| dc.description.abstract | As 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.peerreviewed | No | es_ES |
| dc.format.number | 4 | es_ES |
| dc.format.page | 36-39 | es_ES |
| dc.format.volume | V | es_ES |
| dc.identifier.citation | Boletín del ECEMC: Rev Dismor Epidemiol 2005; V (nº 4): 36-39 | es_ES |
| dc.identifier.issn | 0210–3893 | es_ES |
| dc.identifier.journal | Boletín del ECEMC: Revista de Dismorfología y Epidemiología | es_ES |
| dc.identifier.uri | http://hdl.handle.net/20.500.12105/14002 | |
| dc.language.iso | spa | es_ES |
| dc.publisher | Instituto de Salud Carlos III (ISCIII). Instituto de Investigación de Enfermedades Raras (IIER) | |
| dc.repisalud.centro | ISCIII::Instituto de Investigación de Enfermedades Raras (IIER) | es_ES |
| dc.repisalud.institucion | ISCIII | es_ES |
| dc.rights.accessRights | open access | es_ES |
| dc.rights.license | Atribución-NoComercial-CompartirIgual 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | * |
| dc.subject | Síndrome de macrocefalia-cutis marmorata telangiectásica | es_ES |
| dc.subject | Síndrome de Van der Woude | es_ES |
| dc.subject | Síndrome de Hay-Wells | es_ES |
| dc.subject | Síndrome de Zellweger | es_ES |
| dc.subject | Síndrome de Jeune | es_ES |
| dc.subject | Síndrome de Laurin-Sandrow | es_ES |
| dc.title | Síndromes muy poco frecuentes | es_ES |
| dc.type | research article | es_ES |
| dc.type.hasVersion | VoR | es_ES |
| dspace.entity.type | Publication | |
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| relation.isAuthorOfPublication.latestForDiscovery | 5764d316-caf4-47a6-b03f-4cfdc5b2e892 | |
| relation.isPublisherOfPublication | 13391f4b-b95b-422e-8d68-185598961e13 | |
| relation.isPublisherOfPublication.latestForDiscovery | 13391f4b-b95b-422e-8d68-185598961e13 |
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