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.
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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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