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dc.contributor.authorAraujo Vilar, David 
dc.contributor.authorFernández Pombo, Antía
dc.contributor.authorRodríguez Carnero, María Gemma
dc.contributor.authorMartínez Olmos, Miguel Ángel 
dc.contributor.authorCantón Blanco, Ana 
dc.contributor.authorVillar Taibo, Rocio
dc.contributor.authorHermida Ameijeiras, Alvaro 
dc.contributor.authorSantamaría Nieto, Alicia
dc.contributor.authorDíaz Ortega, Carmen
dc.contributor.authorMartínez Rey, Maria del Carmen
dc.contributor.authorAntela López, Antonio 
dc.contributor.authorLosada Arias, Elena 
dc.contributor.authorMuy Pérez, Andrés Efrain
dc.contributor.authorGonzález Méndez, Blanca
dc.contributor.authorSánchez Iglesias, Sofía
dc.date.accessioned2022-04-29T10:25:36Z
dc.date.available2022-04-29T10:25:36Z
dc.date.issued2020
dc.identifier.issn1750-1172
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/32241282es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16591
dc.description.abstractBACKGROUND: Lipodystrophy syndromes are a group of disorders characterized by a loss of adipose tissue once other situations of nutritional deprivation or exacerbated catabolism have been ruled out. With the exception of the HIV-associated lipodystrophy, they have a very low prevalence, which together with their large phenotypic heterogeneity makes their identification difficult, even for endocrinologists and pediatricians. This leads to significant delays in diagnosis or even to misdiagnosis. Our group has developed an algorithm that identifies the more than 40 rare lipodystrophy subtypes described to date. This algorithm has been implemented in a free mobile application, LipoDDx(R). Our aim was to establish the effectiveness of LipoDDx(R). Forty clinical records of patients with a diagnosis of certainty of most lipodystrophy subtypes were analyzed, including subjects without lipodystrophy. The medical records, blinded for diagnosis, were evaluated by 13 physicians, 1 biochemist and 1 dentist. Each evaluator first gave his/her results based on his/her own criteria. Then, a second diagnosis was given using LipoDDx(R). The results were analysed based on a score table according to the complexity of each case and the prevalence of the disease. RESULTS: LipoDDx(R) provides a user-friendly environment, based on usually dichotomous questions or choice of clinical signs from drop-down menus. The final result provided by this app for a particular case can be a low/high probability of suffering a particular lipodystrophy subtype. Without using LipoDDx(R) the success rate was 17 +/- 20%, while with LipoDDx(R) the success rate was 79 +/- 20% (p < 0.01). CONCLUSIONS: LipoDDx(R) is a free app that enables the identification of subtypes of rare lipodystrophies, which in this small cohort has around 80% effectiveness, which will be of help to doctors who are not experts in this field. However, it will be necessary to analyze more cases in order to obtain a more accurate efficiency value.en
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAdipose Tissue*
dc.subject.meshHumans*
dc.subject.meshSyndrome*
dc.subject.meshRare Diseases*
dc.titleLipoDDx: a mobile application for identification of rare lipodystrophy syndromesen
dc.typeJournal Articlees
dc.authorsophosAraujo-Vilar, D.;Fernandez-Pombo, A.;Rodriguez-Carnero, G.;Martinez-Olmos, M. N.;Canton, A.;Villar-Taibo, R.;Hermida-Ameijeiras, A.;Santamaria-Nieto, A.;Diaz-Ortega, C.;Martinez-Rey, C.;Antela, A.;Losada, E.;Muy-Perez, A. E.;Gonzalez-Mendez, B.;Sanchez-Iglesias, S.
dc.identifier.doi10.1186/s13023-020-01364-1
dc.identifier.pmid32241282
dc.identifier.sophos39495
dc.issue.number1es
dc.journal.titleOrphanet Journal of Rare Diseaseses
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Endocrinoloxíaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Medicina Internaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Santiago de Compostela - Complexo Hospitalario Universitario de Santiago de Compostela::Pediatríaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS)es
dc.rights.accessRightsopenAccess
dc.subject.decsenfermedades raras*
dc.subject.decssíndrome*
dc.subject.decshumanos*
dc.subject.decstejido adiposo*
dc.subject.keywordCHUSes
dc.subject.keywordIDISes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number15es


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Atribución 4.0 Internacional
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