Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/9845
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorCARVALHO, Ellaine-
dc.contributor.authorHONJO, Rachel-
dc.contributor.authorMAGALHAES, Monize-
dc.contributor.authorYAMAMOTO, Guilherme-
dc.contributor.authorROCHA, Katia-
dc.contributor.authorNASLAVSKY, Michel-
dc.contributor.authorZATZ, Mayana-
dc.contributor.authorPASSOS-BUENO, Maria Rita-
dc.contributor.authorKIM, Chong-
dc.contributor.authorBERTOLA, Debora-
dc.date.accessioned2015-08-14T15:39:33Z-
dc.date.available2015-08-14T15:39:33Z-
dc.date.issued2015-
dc.identifier.citationAMERICAN JOURNAL OF MEDICAL GENETICS PART A, v.167A, n.5, p.1039-1046, 2015-
dc.identifier.issn1552-4825-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/9845-
dc.description.abstractSchinzel-Giedion syndrome is a rare autosomal dominant disorder comprising postnatal growth failure, profound developmental delay, seizures, facial dysmorphisms, genitourinary, skeletal, neurological, and cardiac defects. It was recently revealed that Schinzel-Giedion syndrome is caused by de novo mutations in SETBP1, but there are few reports of this syndrome with molecular confirmation. We describe two unrelated Brazilian patients with Schinzel-Giedion syndrome, one of them carrying a novel mutation. We also present a review of clinical manifestations of the syndrome, comparing our cases to patients reported in literature emphasizing the importance of the facial gestalt associated with neurological involvement for diagnostic suspicion of this syndrome. (c) 2015 Wiley Periodicals, Inc.-
dc.language.isoeng-
dc.publisherWILEY-BLACKWELL-
dc.relation.ispartofAmerican Journal of Medical Genetics Part A-
dc.rightsrestrictedAccess-
dc.subjectSchinzel-Giedion syndrome-
dc.subjectclinical features-
dc.subjectfacial gestalt-
dc.subjectSETBP1-
dc.subject.othersacrococcygeal teratoma-
dc.subject.otherneurodegenerative process-
dc.subject.othermidface retraction-
dc.subject.othertumor-
dc.subject.otherhydronephrosis-
dc.subject.otherdelineation-
dc.subject.otherphenotype-
dc.subject.otheranomalies-
dc.subject.othersibs-
dc.titleSchinzel-Giedion Syndrome in Two Brazilian Patients: Report of a Novel Mutation in SETBP1 and Literature Review of the Clinical Features-
dc.typearticle-
dc.rights.holderCopyright WILEY-BLACKWELL-
dc.identifier.doi10.1002/ajmg.a.36789-
dc.identifier.pmid25663181-
dc.subject.wosGenetics & Heredity-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalMAGALHAES, Monize:Univ Sao Paulo, Inst Biociencias, Dept Biol, Ctr Estudos Genoma Humano, Sao Paulo, Brazil-
hcfmusp.author.externalROCHA, Katia:Univ Sao Paulo, Inst Biociencias, Dept Biol, Ctr Estudos Genoma Humano, Sao Paulo, Brazil-
hcfmusp.author.externalNASLAVSKY, Michel:Univ Sao Paulo, Inst Biociencias, Dept Biol, Ctr Estudos Genoma Humano, Sao Paulo, Brazil-
hcfmusp.author.externalZATZ, Mayana:Univ Sao Paulo, Inst Biociencias, Dept Biol, Ctr Estudos Genoma Humano, Sao Paulo, Brazil-
hcfmusp.author.externalPASSOS-BUENO, Maria Rita:Univ Sao Paulo, Inst Biociencias, Dept Biol, Ctr Estudos Genoma Humano, Sao Paulo, Brazil-
hcfmusp.description.beginpage1039-
hcfmusp.description.endpage1046-
hcfmusp.description.issue5-
hcfmusp.description.volume167A-
hcfmusp.origemWOS-
hcfmusp.origem.id2-s2.0-84927761689-
hcfmusp.origem.idWOS:000353171900011-
hcfmusp.publisher.cityHOBOKEN-
hcfmusp.publisher.countryUSA-
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dc.description.indexMEDLINE-
dc.identifier.eissn1552-4833-
hcfmusp.citation.scopus16-
hcfmusp.scopus.lastupdate2022-09-06-
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Artigos e Materiais de Revistas Científicas - FM/MPE
Departamento de Pediatria - FM/MPE

Artigos e Materiais de Revistas Científicas - HC/ICHC
Instituto Central - HC/ICHC

Artigos e Materiais de Revistas Científicas - HC/ICr
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LIM/36 - Laboratório de Pediatria Clínica


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