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dc.contributor.advisorGonzález-Lamuño Leguina, Domingo 
dc.contributor.authorRomero Jiménez, Sergio
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2019-08-07T08:26:35Z
dc.date.available2019-08-07T08:26:35Z
dc.date.issued2019-06
dc.identifier.urihttp://hdl.handle.net/10902/16695
dc.description.abstractIn precision medicine, the focus is on identifying which approaches will be effective for which patients based on genetic, environmental, and lifestyle factors. We present the case of 10 years old child diagnosed with an autism spectrum disorder (ASD) and a corticosensitive, relapsing nephrotic syndrome (NS). When treated with high doses of glucocorticoids for each NS outbreak, the behavioral alterations related to his ASD improved significantly. As we identify an specific genetic alteration in ACTN4, implied not only in the pathogenesis of the NS but also in the cerebral architecture, being included in the genetic panels for the study of ASD, we intend to justify the possible mechanisms that explain the response to glucocorticoid treatment. Based in our rationale, we propose a therapeutic alternative, which could resemble the effects of the corticoid treatment without the secondary effects linked to glucocorticoids.es_ES
dc.format.extent21 p.es_ES
dc.language.isospaes_ES
dc.rights© Sergio Romero Jiménezes_ES
dc.subject.otherAutismes_ES
dc.subject.otherPrecision medicinees_ES
dc.subject.otherBumetanidees_ES
dc.titleAn example of Precision Medicine : possible common molecular mechanisms of disease in a child with Familiar Nephrotic Syndrome and Autism Spectrum Disorder : a proposal of pharmacological treatmentes_ES
dc.title.alternativeUn ejemplo de Medicina de Precisión: posibles mecanismos moleculares comunes causantes de enfermedad en un niño con Síndrome Nefrótico Familiar y Trastorno del Espectro Autista : Propuesta terapéuticaes_ES
dc.typeinfo:eu-repo/semantics/bachelorThesises_ES
dc.rights.accessRightsrestrictedAccesses_ES
dc.description.degreeGrado en Medicinaes_ES


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