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

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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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Ochando, I., Martínez, M. C. A., Serrano, A. M., Urbano, A., Cazorla, E., Calvo, D., & Rueda, J. (2018). Prenatal diagnosis and molecular cytogenetic characterization of a de novo duplication of 15q24.3-q26.1. Application of Clinical Genetics, 11, 77–80. https://doi.org/10.2147/TACG.S159377

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