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dc.contributor.authorMuschol, Nicolept_BR
dc.contributor.authorGiugliani, Robertopt_BR
dc.contributor.authorJones, Simon A.pt_BR
dc.contributor.authorMuenzer, Josephpt_BR
dc.contributor.authorSmith, Nicholas J. C.pt_BR
dc.contributor.authorWhitley, Chester B.pt_BR
dc.contributor.authorDonnell, Meganpt_BR
dc.contributor.authorDrake, Elisept_BR
dc.contributor.authorElvidge, Kristinapt_BR
dc.contributor.authorMelton, Lisapt_BR
dc.contributor.authorO’Neill, Carapt_BR
dc.date.accessioned2023-03-10T03:27:11Zpt_BR
dc.date.issued2022pt_BR
dc.identifier.issn1750-1172pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/255561pt_BR
dc.description.abstractSanfilippo syndrome is a group of rare, complex, and progressive neurodegenerative lysosomal storage disorders that is characterized by childhood dementia. The clinical management of patients with progressive neurological decline and multisystem involvement requires a multidisciplinary team with experience in the management of neurodegenerative disorders. Best practice guidelines for the clinical management of patients with these types of rare disorders are critical to ensure prompt diagnosis and initiation of appropriate care. However, there are no published standard global clinical care guidelines for patients with Sanfilippo syndrome. To address this, a literature review was conducted to evaluate the current evidence base and to identify evidence gaps. The findings were reviewed by an international steering committee composed of clinical experts with extensive experience in managing patients with Sanfilippo syndrome. The goal was to create a consensus set of basic clinical guidelines that will be accessible to and informed by clinicians globally, as well as providing a practical resource for families to share with their local care team who may not have experience with this rare disease. This review distills 178 guideline statements into an easily digestible document that provides evidence-based, expert-led recommendations for how to approach common management challenges and appropriate monitoring schedules in the care of patients with Sanfilippo syndrome.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofOrphanet journal of rare diseases. [London]. Vol. 17 (2022), 391, 23 p.pt_BR
dc.rightsOpen Accessen
dc.subjectMucopolissacaridose IIIpt_BR
dc.subjectMucopolysaccharidosis type IIIen
dc.subjectSanflippo syndromeen
dc.subjectDiagnósticopt_BR
dc.subjectDiagnosisen
dc.subjectAtenção à saúdept_BR
dc.subjectManagementen
dc.subjectRecommendationsen
dc.titleSanfilippo syndrome : consensus guidelines for clinical carept_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001160899pt_BR
dc.type.originEstrangeiropt_BR


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