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dc.contributor.authorMartínez-Frías, María Luisa 
dc.contributor.authorBermejo-Sanchez, Eva 
dc.contributor.authorLópez Grondona, Fermín 
dc.contributor.authorRodríguez-Pinilla, Elvira 
dc.contributor.authorMendioroz, J
dc.contributor.authorCuevas Catalina, María Lourdes 
dc.contributor.authorBarcia, JM
dc.contributor.authorOliván del Cacho, MJ
dc.contributor.authorEspinosa, MJ
dc.contributor.authorGómez, F
dc.contributor.authorAparicio, P
dc.contributor.authorFélix, V
dc.contributor.authorGarcía, A
dc.contributor.authorGarcía, MJ
dc.contributor.authorVázquez, MS
dc.contributor.authorCenteno, F
dc.contributor.authorGarcía, MM
dc.contributor.authorMarco, JJ
dc.contributor.authorGalán, E
dc.contributor.authorGómez, H
dc.contributor.authorBlanco, M
dc.contributor.authorLópez Soler, JA
dc.contributor.authorPaisán L
dc.date.accessioned2022-02-22T11:28:21Z
dc.date.available2022-02-22T11:28:21Z
dc.date.issued2004-10
dc.identifier.citationBoletín del ECEMC: Rev Dismor Epidemiol 2004; V (nº 3): 2-13es_ES
dc.identifier.issn0210–3893es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/13698
dc.descriptionDismorfología, Citogenética y Clínica: Resultados de estudios sobre los datos del ECEMCes_ES
dc.description.abstractThe Ichthyoses constitutes a large family of genetic skin diseases characterized by dry skin and variable degrees of blisters and scales. There are at least twenty varieties of ichthyosis, with a wide range of severity and associated symptoms, and genetic heterogeneity (autosomal dominant, autosomal recessive, and X-linked inheritance). The clinical symptoms, which are non-specific, may not be apparent. We have attempted to provide a classification of the ichthyoses and some guidance for the diagnosis and management of these conditions. The present classification is based in the type of alteration of the skin layer, the molecular findings, the biochemical characteristics, and the family history.There are three main categories, which include different subgroups of ichthyoses: 1) Those that are caused by an altered process of keratinocytic diferenciation (altered intermediate filaments/keratins). This category includes the following subgroups: a) Harlequin fetus; b) bullous erythroderma ichthyosiformis congenital; c) Ichthyosis bullosa of Siemens; d) Ichthyosis hystrix of Curth-Macklin; and e) Ichthyosis vulgaris. 2) Those that are caused by a deficient formation of the cornified envelope (transglutaminase 1 enzyme deficiency). In this category we include two main subgrups: a) Lamellar ichthyosis AR, which includes i) ichthyosis lamellar (IL1, IL2, IL3, IL4, and IL5), and ii) ichthyosiform erythroderma congenital nonbullous, and b) Nonlamellar ichthyosis and nonerythrodermic congenital ichthyosis AR. 3) Those caused by an abnormal steroid sulfatase (X-linked Ichtyosis). In spite of having only data at birth and the lack of molecular analysis, we attempted to classify the ECEMC cases according to this classification using available clinical data. We also calculated the frequency of this disease identified at birth, and provide some guidance for the clinical diagnosis, the management of the affected newborn, and the information that should be offered to the parents.es_ES
dc.language.isospaes_ES
dc.publisherInstituto de Salud Carlos III (ISCIII). Instituto de Investigación de Enfermedades Raras (IIER) es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subjectDismorfologíaes_ES
dc.subjectAnomalías congénitases_ES
dc.subjectEpidemiologíaes_ES
dc.subjectIchthyosises_ES
dc.subjectCollodion babyes_ES
dc.subjectHarlequin fetuses_ES
dc.subjectFrequencyes_ES
dc.subjectEtiologyes_ES
dc.titleAspectos diagnósticos, etiológicos y genéticos de las ictiosis congénitas al nacimientoes_ES
dc.title.alternativeDiagnostic, etiologic, and genetic aspects of congenital ichthyoses at birth: Characteristics of the ECEMC caseses_ES
dc.typejournal articlees_ES
dc.rights.licenseAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.format.volumeVes_ES
dc.format.number3es_ES
dc.format.page2-13es_ES
dc.description.peerreviewedNoes_ES
dc.identifier.journalBoletín del ECEMC: Revista de Dismorfología y Epidemiologíaes_ES
dc.repisalud.centroISCIIIes_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES


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Atribución-NoComercial-CompartirIgual 4.0 Internacional
Este Item está sujeto a una licencia Creative Commons: Atribución-NoComercial-CompartirIgual 4.0 Internacional