Manejo clínico de la epidermolisis ampollosa distrófica hereditaria: a propósito de un caso.
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| Title: | Manejo clínico de la epidermolisis ampollosa distrófica hereditaria: a propósito de un caso. |
|---|---|
| Alternate Title: | Clinical handling of hereditary dystrophic epidermolysis bullosa: a case report. |
| Authors: | Fagoaga, L. Blanquer1 laurblan@hotmail.com, García, B. Garrido1, Casimiro, L. Martínez1, Andreu, M. Romero1 |
| Source: | Acta Pediátrica Española. ene2012, Vol. 70 Issue 1, p31-34. 4p. |
| Subjects: | EPIDERMOLYSIS bullosa, GENETIC disorders, BLISTERS, IRRITATION (Pathology), SKIN diseases |
| Abstract (English): | The epidermolysis bullosa constitute a group of determined genetically illnesses characterized by an excessive fragility of the skin to the friction forces. All of them take place for protein alterations, today known, that intervene in the union of the epidermis with the dermis. This leads to the formation of erosion and blisters, spontaneously or before a minimal traumatism. The patients suffering from this type of pathologies need a very careful clinical handling, which propitiates them the attention adapted to support a good quality of life, as well as the prevention and opportune treatment of the multiple complications that they can present, some of which can go so far as to threaten their life. We present of dystrophic epidermolysis bullosa case at birth, confirmed throughout histological and ultrastructural studies. [ABSTRACT FROM AUTHOR] |
| Abstract (Spanish): | Las epidermolisis ampollosas son enfermedades genéticamente determinadas, caracterizadas por una fragilidad excesiva de la piel a las fuerzas de fricción. Esto ocasiona erosiones y ampollas, espontáneamente o ante mínimos traumatismos. Todas ellas se producen por alteraciones, hoy conocidas, en las proteínas de la unión dermoepidérmica. Los pacientes afectados requieren una atención adecuada para mantener una buena calidad de vida, mediante un manejo clínico muy cuidadoso, que incluya la prevención y el tratamiento oportuno de las múltiples complicaciones asociadas, algunas de las cuales pueden llegar a condicionar su supervivencia. Presentamos un caso de epidermolisis ampollosa distrófica con inicio en el nacimiento, confirmada con estudios histológicos y ultraestructurales. [ABSTRACT FROM AUTHOR] |
| Copyright of Acta Pediátrica Española is the property of Ediciones Mayo and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | MedicLatina |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: lth DbLabel: MedicLatina An: 82330746 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Manejo clínico de la epidermolisis ampollosa distrófica hereditaria: a propósito de un caso. – Name: TitleAlt Label: Alternate Title Group: TiAlt Data: Clinical handling of hereditary dystrophic epidermolysis bullosa: a case report. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Fagoaga%2C+L%2E+Blanquer%22">Fagoaga, L. Blanquer</searchLink><relatesTo>1</relatesTo><i> laurblan@hotmail.com</i><br /><searchLink fieldCode="AR" term="%22García%2C+B%2E+Garrido%22">García, B. Garrido</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Casimiro%2C+L%2E+Martínez%22">Casimiro, L. Martínez</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Andreu%2C+M%2E+Romero%22">Andreu, M. Romero</searchLink><relatesTo>1</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Acta+Pediátrica+Española%22">Acta Pediátrica Española</searchLink>. ene2012, Vol. 70 Issue 1, p31-34. 4p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22EPIDERMOLYSIS+bullosa%22">EPIDERMOLYSIS bullosa</searchLink><br /><searchLink fieldCode="DE" term="%22GENETIC+disorders%22">GENETIC disorders</searchLink><br /><searchLink fieldCode="DE" term="%22BLISTERS%22">BLISTERS</searchLink><br /><searchLink fieldCode="DE" term="%22IRRITATION+%28Pathology%29%22">IRRITATION (Pathology)</searchLink><br /><searchLink fieldCode="DE" term="%22SKIN+diseases%22">SKIN diseases</searchLink> – Name: Abstract Label: Abstract (English) Group: Ab Data: The epidermolysis bullosa constitute a group of determined genetically illnesses characterized by an excessive fragility of the skin to the friction forces. All of them take place for protein alterations, today known, that intervene in the union of the epidermis with the dermis. This leads to the formation of erosion and blisters, spontaneously or before a minimal traumatism. The patients suffering from this type of pathologies need a very careful clinical handling, which propitiates them the attention adapted to support a good quality of life, as well as the prevention and opportune treatment of the multiple complications that they can present, some of which can go so far as to threaten their life. We present of dystrophic epidermolysis bullosa case at birth, confirmed throughout histological and ultrastructural studies. [ABSTRACT FROM AUTHOR] – Name: Abstract Label: Abstract (Spanish) Group: Ab Data: Las epidermolisis ampollosas son enfermedades genéticamente determinadas, caracterizadas por una fragilidad excesiva de la piel a las fuerzas de fricción. Esto ocasiona erosiones y ampollas, espontáneamente o ante mínimos traumatismos. Todas ellas se producen por alteraciones, hoy conocidas, en las proteínas de la unión dermoepidérmica. Los pacientes afectados requieren una atención adecuada para mantener una buena calidad de vida, mediante un manejo clínico muy cuidadoso, que incluya la prevención y el tratamiento oportuno de las múltiples complicaciones asociadas, algunas de las cuales pueden llegar a condicionar su supervivencia. Presentamos un caso de epidermolisis ampollosa distrófica con inicio en el nacimiento, confirmada con estudios histológicos y ultraestructurales. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Acta Pediátrica Española is the property of Ediciones Mayo and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Languages: – Code: spa Text: Spanish PhysicalDescription: Pagination: PageCount: 4 StartPage: 31 Subjects: – SubjectFull: EPIDERMOLYSIS bullosa Type: general – SubjectFull: GENETIC disorders Type: general – SubjectFull: BLISTERS Type: general – SubjectFull: IRRITATION (Pathology) Type: general – SubjectFull: SKIN diseases Type: general Titles: – TitleFull: Manejo clínico de la epidermolisis ampollosa distrófica hereditaria: a propósito de un caso. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Fagoaga, L. Blanquer – PersonEntity: Name: NameFull: García, B. Garrido – PersonEntity: Name: NameFull: Casimiro, L. Martínez – PersonEntity: Name: NameFull: Andreu, M. Romero IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: ene2012 Type: published Y: 2012 Identifiers: – Type: issn-print Value: 00016640 Numbering: – Type: volume Value: 70 – Type: issue Value: 1 Titles: – TitleFull: Acta Pediátrica Española Type: main |
| ResultId | 1 |
