1. RIUdeG
  2. Repositorios RedUdeG
  3. CUALTOS
Por favor, use este identificador para citar o enlazar este ítem: https://hdl.handle.net/20.500.12104/72550
Registro completo de metadatos
Campo DCValorLengua/Idioma
dc.creatorMacías Gómez, Nelly Margarita-
dc.creatorLeal Ugarte, Evelia-
dc.creatorGutiérrez Angulo, Melva-
dc.creatorDomínguez Quezada, Guadalupe-
dc.creatorRivera, Horacio-
dc.creatorBarros Núñez, Patricio-
dc.date2015-07-21T19:22:23Z-
dc.date2015-07-21T19:22:23Z-
dc.date2012-09-
dc.date.accessioned2019-04-07T23:47:54Z-
dc.date.available2019-04-07T23:47:54Z-
dc.identifierMacías-Gómez, N., Leal-Ugarte, E., Gutiérrez-Angulo, M., Domínguez-Quezada, G., Rivera, H., & Barros-Núñez, P. (2012). 46,XX ovotesticular disorder in a Mexican patient with Beckwith–Wiedemann syndrome: a case report. Journal of Medical Case Reports, 6(1), 301. http://doi.org/10.1186/1752-1947-6-301-
dc.identifier1752-1947-
dc.identifierdoi:10.1186/1752-1947-6-301-
dc.identifierhttp://repositorio.cualtos.udg.mx:8080/jspui/handle/123456789/352-
dc.identifier.urihttps://hdl.handle.net/20.500.12104/72550-
dc.descriptionIntroduction Beckwith–Wiedemann syndrome is an overgrowth syndrome that is characterized by hypoglycemia at birth, coarse face, hemihypertrophy and an increased risk to develop embryonal tumors. In approximately 15% of patients, the inheritance is autosomal dominant with variable expressivity and incomplete penetrance, whereas the remainder of Beckwith–Wiedemann syndrome cases are sporadic. Beckwith–Wiedemann syndrome molecular etiologies are complex and involve the two imprinting centers 1 (IC1) and 2 (IC2) of 11p15 region. This case report describes, for the first time, the unusual association of ovotesticular disorder in a patient from Morelia, Mexico with Wiedemann-Beckwith syndrome. Case presentation We report the case of a Mexican six-year-old girl with Beckwith–Wiedemann Syndrome, ambiguous genitalia, and bilateral ovotestes. She has a 46,XX karyotype without evidence of Y-chromosome sequences detected by fluorescence in situ hybridization with both SRY and wcp-Y probes. Conclusion Although a random association between these two conditions cannot be excluded, future analysis of this patient with Beckwith–Wiedemann syndrome and 46,XX ovotesticular disorder may lead to new insights into these complex pathologies. We speculate that a possible misregulation in the imprinted genes network has a fundamental role in the coexistence of these two disorders.-
dc.descriptionDepartamento de Salud y Bienestar, Centro Universitario del Sur, U de G., Ciudad Guzmán, Jalisco, Mexico. Unidad Académica de Ciencias de la Salud y Tecnología, UAT, Matamoros, Tamps, Mexico. Centro Universitario de Los Altos, U de G, Tepatitlán de Morelos, Jalisco, Mexico. Centro de Investigación Biomédica de Occidente-IMSS, Guadalajara, Jalisco, Mexico.-
dc.languageen-
dc.publisherJournal of Medical Case Reports.-
dc.relationJournal of Medical Case Reports;6:301-
dc.subjectovotesticular disorder-
dc.subjectBeckwith–Wiedemann syndrome-
dc.title46,XX ovotesticular disorder in a Mexican patient with Beckwith–Wiedemann syndrome: a case report.-
dc.typeArticle-
Aparece en las colecciones:CUALTOS

Ficheros en este ítem:
No hay ficheros asociados a este ítem.
Mostrar el registro sencillo del ítem


Los ítems de RIUdeG están protegidos por copyright, con todos los derechos reservados, a menos que se indique lo contrario.