Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/39899
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dc.contributor.authorGarcía-Cruz, D.
dc.contributor.authorMampel, A.
dc.contributor.authorEcheverria, M.I.
dc.contributor.authorVargas, A.L.
dc.contributor.authorCastaneda-Cisneros, G.
dc.contributor.authorDavalos-Rodriguez, N.
dc.contributor.authorPatino-García, B.
dc.contributor.authorGarcía-Cruz, M.O.
dc.contributor.authorCastaneda, V.
dc.contributor.authorCardona, E.G.
dc.contributor.authorMarin-Solis, B.
dc.contributor.authorCantu, J.M.
dc.contributor.authorNunez-Reveles, N.
dc.contributor.authorMoran-Moguel, C.
dc.contributor.authorThavanati, P.K.R.
dc.contributor.authorRamirez-García, S.
dc.contributor.authorSanchez-Corona, J.
dc.date.accessioned2015-09-15T17:28:02Z-
dc.date.available2015-09-15T17:28:02Z-
dc.date.issued2011
dc.identifier.urihttp://hdl.handle.net/20.500.12104/39899-
dc.identifier.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-78650789392&partnerID=40&md5=9a20a2318f26afe642406d9567624b6a
dc.identifier.urihttp://ovidsp.ovid.com/ovidweb.cgi?T=JS&CSC=Y&NEWS=N&PAGE=fulltext&D=medl&AN=20890180
dc.description.abstractThree female patients with Cantu syndrome were studied, two of whom were adults presenting with the complication of lymphoedema, as described earlier in a male patient with this syndrome. The aim of this study is to report the clinical characteristics of these three new cases and to emphasize that lymphoedema, as observed in two of the patients described here, has been observed in 11.5% of patients with Cantu syndrome and that heterochromia iridis, observed in one patient, is probably a new feature of this condition. Zapotitlán 2011 Wolters Kluwer Health. Lippincott Williams & Wilkins.
dc.relation.isreferencedbyScopus
dc.relation.isreferencedbyWOS
dc.relation.isreferencedbyMEDLINE
dc.titleCantu syndrome and lymphoedema
dc.typeArticle
dc.identifier.doi10.1097/MCD.0b013e32833d015c
dc.relation.ispartofjournalClinical Dysmorphology
dc.relation.ispartofvolume20
dc.relation.ispartofissue1
dc.relation.ispartofpage32
dc.relation.ispartofpage37
dc.subject.keywordCantu syndrome; congenital generalized hypertrichosis; heterochromia iridis; lymphoedema; Genetics & Heredity
dc.contributor.affiliationGarcía-Cruz, D., Instituto de Genetica Humana 'Dr Enrique Corona Rivera', Departamento de Biologia Molecular y Genomica, Universidad de Guadalajara, Sierra Mojada 950, Edificio P, Nivel 2, Col. Independencia, Guadalajara CP 44340, Jalisco, Mexico; Mampel, A., Instituto de Genetica, Facultad de Ciencias Medicas, Universidad Nacional de Cuyo, Mendoza, Argentina; Echeverria, M.I., Instituto de Genetica, Facultad de Ciencias Medicas, Universidad Nacional de Cuyo, Mendoza, Argentina; Vargas, A.L., Instituto de Genetica, Facultad de Ciencias Medicas, Universidad Nacional de Cuyo, Mendoza, Argentina; Castañeda-Cisneros, G., Hospital de Especialidades, CMNO, Mexico; Davalos-Rodriguez, N., Instituto de Genetica Humana 'Dr Enrique Corona Rivera', Departamento de Biologia Molecular y Genomica, Universidad de Guadalajara, Sierra Mojada 950, Edificio P, Nivel 2, Col. Independencia, Guadalajara CP 44340, Jalisco, Mexico; Patiño-García, B., Division de Medicina Molecular, CIBO, CMNO, Mexico; García-Cruz, M.O., Hospital General Regional 46, Mexico; Castañeda, V., Hospital de Especialidades, CMNO, Mexico; Cardona, E.G., Hospital General Regional 45, IMSS, Guadalajara, Jalisco, Mexico; Marin-Solis, B., Hospital de Especialidades, CMNO, Mexico; Cantu, J.M., Instituto de Genetica Humana 'Dr Enrique Corona Rivera', Departamento de Biologia Molecular y Genomica, Universidad de Guadalajara, Sierra Mojada 950, Edificio P, Nivel 2, Col. Independencia, Guadalajara CP 44340, Jalisco, Mexico; Nuñez-Reveles, N., Instituto de Genetica Humana 'Dr Enrique Corona Rivera', Departamento de Biologia Molecular y Genomica, Universidad de Guadalajara, Sierra Mojada 950, Edificio P, Nivel 2, Col. Independencia, Guadalajara CP 44340, Jalisco, Mexico; Moran-Moguel, C., Division de Medicina Molecular, CIBO, CMNO, Mexico; Thavanati, P.K.R., Instituto de Genetica Humana 'Dr Enrique Corona Rivera', Departamento de Biologia Molecular y Genomica, Universidad de Guadalajara, Sierra Mojada 950, Edificio P, Nivel 2, Col. Independencia, Guadalajara CP 44340, Jalisco, Mexico; Ramirez-García, S., Instituto de Enfermedades Cronico-Degenerativas, Departamento de Biologia Molecular y Genomica, Universidad de Guadalajara, Mexico; Sanchez-Corona, J., Division de Medicina Molecular, CIBO, CMNO, Mexico
dc.subject.headingIndex Medicus;Adult;Cardiomegaly/co [Complications];Cardiomegaly/ra [Radiography];Child;Child, Preschool;Genetic Diseases, X-Linked/co [Complications];Genetic Diseases, X-Linked/ra [Radiography];Humans;Hypertrichosis/co [Complications];Hypertrichosis/ra [Radiography];Infant;Infant, Newborn;Lymphatic System/pa [Pathology];Lymphedema/co [Complications];Lymphedema/ra [Radiography];Lymphography;Male;Osteochondrodysplasias/co [Complications];Osteochondrodysplasias/ra [Radiography];Ribs/ra [Radiography];Young Adult
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