Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/1794
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dc.contributor.authorBarbero, Pabloes
dc.contributor.authorLotersztein, Vanesaes
dc.contributor.authorBronberg, Rubénes
dc.contributor.authorPerez, Miriames
dc.contributor.authorAlba, Lilianaes
dc.date.accessioned2020-12-02T14:28:15Z-
dc.date.available2020-12-02T14:28:15Z-
dc.date.issued2004-10-
dc.identifier.issn1542-0752-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/1794-
dc.descriptionFil: Barbero, Pablo. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.es
dc.descriptionFil: Lotersztein, Vanesa. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.es
dc.descriptionFil: Bronberg, Ruben. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.es
dc.descriptionFil: Perez, Miriam. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.es
dc.descriptionFil: Alba, Liliana. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.es
dc.description.abstractAcitretin is an aromatic retinoid analog of vitamin A. Drugs of this group are well-known teratogenic agents. Nevertheless, acitretin embryopathy has been described only in fetuses. CASE: An infant was exposed to 10 mg/day of acitretin from the beginning of pregnancy until the 10th gestational week. At term, the newborn showed the following abnormalities: microcephaly, epicanthal folds, low nasal bridge, high palate, cup-shaped ears, anteverted nostrils, atrial septal defect, and bilateral sensorineural deafness. At 18 months of age, the patient showed microcephaly and neurodevelopmental delay. CONCLUSIONS: Our patient shows a pattern of anomalies resembling that observed in isotretinoin- and etretinate-exposed children. After ingestion, acitretin is partially converted into etretinate, and etretinate is partially metabolized into acitretin. A similar phenotype would therefore be expected after prenatal exposure to either drug. Moreover, in the present case, teratogenic effects were observed even though the dose was lower than in the previously reported acitretin embryopathy cases. Therefore, we propose that different retinoids, acitretin included, produce only one malformation pattern with variable phenotypic expressiones
dc.language.isoenes
dc.relation.ispartofBirth defects research. Part A, Clinical and molecular teratologyes
dc.rightsClosed Access-
dc.subjectAnomalías Múltipleses
dc.subjectAcitretinaes
dc.subjectEmbrión de Mamíferoses
dc.subjectPérdida Auditivaes
dc.subjectTeratógenoses
dc.titleAcitretin embryopathy: a case reportes
dc.typeArtículoes
dc.identifier.doi10.1002/bdra.20078-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairetypeArtículo-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptCentro Nacional de Genética Médica (CeNaGeM)-
crisitem.author.deptRegistro Nacional de Anomalías Congénitas (RENAC)-
crisitem.author.parentorgAdministración Nacional de Laboratorios e Institutos de Salud “Dr. Carlos G. Malbrán” (ANLIS)-
crisitem.author.parentorgInstituto Nacional de Epidemiología (INE)-
Appears in Collections:Publicaciones CeNaGeM
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