Please use this identifier to cite or link to this item: https://hdl.handle.net/11000/37755

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

Title:
Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 15q24.3-q26.1
Authors:
Ochando, Isabel  
Alonzo Martínez, Melanie Cristine  
Serrano, Ana María
Urbano, Antonio  
Cazorla, Eduardo  
Calvo, Dolores
Rueda, Joaquín  
Editor:
Taylor and Francis. Group Dove Press
Department:
Departamentos de la UMH::Histología y Anatomía
Issue Date:
2018-07
URI:
https://hdl.handle.net/11000/37755
Abstract:
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.
Keywords/Subjects:
distal 15q trisomy
prenatal diagnosis
short limbs
Knowledge area:
CDU: Ciencias aplicadas: Medicina
Type of document:
info:eu-repo/semantics/article
Access rights:
info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
DOI:
https://doi.org/10.2147/TACG.S159377
Published in:
The application of clinical genetics. 2018 Jul 3:11:77-80
Appears in Collections:
Artículos Histología y Anatomía



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