Publication: Acondroplasia: actualización en diagnóstico, seguimiento y tratamiento
dc.contributor.author | Leiva-Gea, Antonio | |
dc.contributor.author | Martos-Lirio, Maria F. | |
dc.contributor.author | Barreda-Bonis, Ana Coral | |
dc.contributor.author | Marin-del-Barrio, Silvia | |
dc.contributor.author | Heath, Karen E. | |
dc.contributor.author | Marin-Reina, Purificacion | |
dc.contributor.author | Guillen-Navarro, Encarna | |
dc.contributor.author | Santos-Simarro, Fernando | |
dc.contributor.author | Riano-Galan, Isolina | |
dc.contributor.author | Yeste-Fernandez, Diego | |
dc.contributor.author | Leiva-Gea, Isabel | |
dc.contributor.authoraffiliation | [Leiva-Gea, Antonio] Hosp Univ Virgen Victoria, UGC Cirugia Ortoped & Traumatol, Inst Invest Biomed Malaga IBIMA Plataforma Bionand, Malaga, Spain | |
dc.contributor.authoraffiliation | [Leiva-Gea, Isabel] Hosp Univ Virgen Victoria, UGC Cirugia Ortoped & Traumatol, Inst Invest Biomed Malaga IBIMA Plataforma Bionand, Malaga, Spain | |
dc.contributor.authoraffiliation | [Lirio, Maria F. Martos] Hosp Reg Malaga, Unidad Endocrinol Pediat, Malaga, Spain | |
dc.contributor.authoraffiliation | [Bonis, Ana Coral Barreda] Hosp Univ La Paz, Serv Endorinol Infantil, Madrid, Spain | |
dc.contributor.authoraffiliation | [Bonis, Ana Coral Barreda] Hosp Univ La Paz, Unidad multidisciplinar displasias esquelet UMDE E, Madrid, Spain | |
dc.contributor.authoraffiliation | [del Barrio, Silvia Marin] Hosp San Joan de Deu, Unidad Endocrinol Pediat, Barcelona, Spain | |
dc.contributor.authoraffiliation | [Heath, Karen E.] Hosp Univ La Paz, Inst Genet Med & Mol INGEMM, IdiPAZ & UMDE ERN BOND, Madrid, Spain | |
dc.contributor.authoraffiliation | [Fernandez, Diego Yeste] Hosp Univ La Paz, Inst Genet Med & Mol INGEMM, IdiPAZ & UMDE ERN BOND, Madrid, Spain | |
dc.contributor.authoraffiliation | [Lirio, Maria F. Martos] Hosp Univ & Politecn La Fe, Unidad Dismorfol & Genet Reprod, Valencia, Spain | |
dc.contributor.authoraffiliation | [Guillen-Navarro, Encarna] Univ Murcia, Serv Genet Med, Serv Pediat, IMIB Pascual Parrilla,Hosp Clin Univ Virgen Arrixa, Murcia, Spain | |
dc.contributor.authoraffiliation | [Simarro, Fernando Santos] Hosp Univ Son Espases, Unidad Diagnost Mol & Genet Clin, Idisba, Palma De Mallorca, Spain | |
dc.contributor.authoraffiliation | [Galan, Isolina Riano] Hosp Reg Malaga, Unidad Endocrinol Pediat, Inst Invest Biomed Malaga Plataforma Bionand, HUCA,CIBERESP, Malaga, Spain | |
dc.contributor.authoraffiliation | [Fernandez, Diego Yeste] Univ Autonoma Barcelona, Hosp Univ Vall Hebron, Serv Endocrinol Pediat, Barcelona, Spain | |
dc.contributor.authoraffiliation | [Leiva-Gea, Isabel] Hosp Reg Malaga, Inst Invest Biomed Malaga Plataforma Bionand, Unidad Endocrinol Pediat, Malaga, Spain | |
dc.date.accessioned | 2023-05-03T14:43:19Z | |
dc.date.available | 2023-05-03T14:43:19Z | |
dc.date.issued | 2022-10-17 | |
dc.description.abstract | La acondroplasia requiere un seguimiento multidisciplinario, con el objetivo de prevenir y manejar las complicaciones, mejorar la calidad de vida y favorecer su independencia e inclusión social. Esta revisión se justifica por las múltiples publicaciones generadas en los últimos años que han llevado a cabo un cambio en su gestión. Se han desarrollado diferentes guías y recomendaciones, entre las que destacan la realizada por la Academia Americana de Pediatría en 2005, recientemente actualizada (2020), la guía japonesa (2020), el primer Consenso Europeo (2021) y el Consenso Internacional sobre el diagnóstico, abordaje, enfoque multidisciplinario y manejo de individuos con acondroplasia a lo largo de la vida (2021). Sin embargo, y a pesar de estas recomendaciones, actualmente existe una gran variabilidad a nivel mundial en el manejo de las personas con acondroplasia, con consecuencias médicas, funcionales y psicosociales en los pacientes y sus familias. Por ello, es fundamental integrar estas recomendaciones en la práctica clínica diaria, teniendo en cuenta la situación particular de cada sistema sanitario. © 2022 Asociación Española de Pediatría. | |
dc.description.abstract | Achondroplasia requieres a multidisciplinary follow-up, with the aim of preventing and managing complications, improving the quality of life and favoring their independence and social inclusion. This review is justified by the multiple publications generated in recent years that have carried out a change in its management. Different guidelines and recommendations have been developed, among which the one made by the American Academy of Pediatrics in 2005 recently updated (2020), the Japanese guide (2020), the first European Consensus (2021) and the International Consensus on the diagnosis, approach multidisciplinary approach and management of individuals with achondroplasia throughout life (2021). However, and despite these recommendations, there is currently a great worldwide variability in the management of people with achondroplasia, with medical, functional and psychosocial consequences in patients and their families. Therefore, it is essential to integrate these recommendations into daily clinical practice, taking into account the particular situation of each health system.(c) 2022 Asociacion Espanola de Pediatria. | |
dc.description.version | Si | |
dc.identifier.citation | Leiva-Gea, A., Lirio, M. F. M., Bonis, A. C. B., Del Barrio, S. M., Heath, K. E., Reina, P. M., et al. (2022). Acondroplasia: actualización en diagnóstico, seguimiento y tratamiento. Anales de Pediatría, 97(6), 423-423.e10 | |
dc.identifier.doi | 10.1016/j.anpedi.2022.10.004 | |
dc.identifier.essn | 1695-9531 | |
dc.identifier.issn | 1695-4033 | |
dc.identifier.unpaywallURL | https://doi.org/10.1016/j.anpedi.2022.10.004 | |
dc.identifier.uri | http://hdl.handle.net/10668/21968 | |
dc.identifier.wosID | 933109900009 | |
dc.issue.number | 6 | |
dc.journal.title | Anales de pediatria | |
dc.journal.titleabbreviation | An. pediatr. | |
dc.language.iso | es | |
dc.organization | Hospital Universitario Virgen de la Victoria | |
dc.organization | Hospital Universitario Regional de Málaga | |
dc.organization | Centro Andaluz de Nanomedicina y Biotecnología-BIONAND | |
dc.organization | Instituto de Investigación Biomédica de Málaga-IBIMA | |
dc.page.number | 11 | |
dc.provenance | Realizada la curación de contenido 06/03/2025 | |
dc.publisher | Elsevier | |
dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S1695403322002284 | |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Achondroplasia | |
dc.subject | Bone dysplasia | |
dc.subject | FGFR3 | |
dc.subject | Children | |
dc.subject | Growth | |
dc.subject | Charts | |
dc.subject | Acondroplasia | |
dc.subject | Displasia ósea | |
dc.subject | FGFR3 | |
dc.subject.decs | Acondroplasia | |
dc.subject.decs | Consenso | |
dc.subject.decs | Sistemas de salud | |
dc.subject.decs | Pediatría | |
dc.subject.decs | Inclusión social | |
dc.subject.mesh | Consensus | |
dc.subject.mesh | Quality of Life | |
dc.subject.mesh | Social Inclusion | |
dc.subject.mesh | Follow-Up Studies | |
dc.subject.mesh | Achondroplasia | |
dc.title | Acondroplasia: actualización en diagnóstico, seguimiento y tratamiento | |
dc.title.alternative | Achondroplasia: Update on diagnosis, follow-up and treatment | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 97 | |
dc.wostype | Article | |
dspace.entity.type | Publication |
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