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Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 15q24.3-q26.1


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Título :
Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 15q24.3-q26.1
Autor :
Ochando, Isabel  
Alonzo Martínez, Melanie Cristine  
Serrano, Ana María
Urbano, Antonio  
Cazorla, Eduardo  
Calvo, Dolores
Rueda, Joaquín  
Editor :
Taylor and Francis. Group Dove Press
Departamento:
Departamentos de la UMH::Histología y Anatomía
Fecha de publicación:
2018-07
URI :
https://hdl.handle.net/11000/37755
Resumen :
Reported cases of distal 15q interstitial duplications are uncommon and do not result in a recognizable pattern of abnormalities. Some studies report prenatal overgrowth, while others describe growth retardation. We present molecular cytogenetic characterization of a 14 Mb interstitial duplication, encompassing 81 Online Mendelian Inheritance in Man (OMIM) genes, in a fetus with single umbilical artery and short limbs. We propose that growth restriction, previously described and present in our patient, may be due to duplication of a gene or genes contained in the 15q24 region.
Palabras clave/Materias:
distal 15q trisomy
prenatal diagnosis
short limbs
Área de conocimiento :
CDU: Ciencias aplicadas: Medicina
Tipo de documento :
info:eu-repo/semantics/article
Derechos de acceso:
info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
DOI :
https://doi.org/10.2147/TACG.S159377
Publicado en:
The application of clinical genetics. 2018 Jul 3:11:77-80
Aparece en las colecciones:
Artículos Histología y Anatomía



Creative Commons La licencia se describe como: Atribución-NonComercial-NoDerivada 4.0 Internacional.