Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability

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Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability

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Title: Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability
Author: Zhang, Shujie; Qin, Haisong; Wang, Jin; OuYang, Luping; Luo, Shiyu; Fu, Chunyun; Fan, Xin; Su, Jiasun; Chen, Rongyu; Xie, Bobo; Hu, Xuyun; Chen, Shaoke; Shen, Yiping

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Citation: Zhang, S., H. Qin, J. Wang, L. OuYang, S. Luo, C. Fu, X. Fan, et al. 2016. “Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability.” Molecular Cytogenetics 9 (1): 66. doi:10.1186/s13039-016-0274-4. http://dx.doi.org/10.1186/s13039-016-0274-4.
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Abstract: Background: Both maternal uniparental disomy 14 (UPD(14)mat) and mosaic trisomy 14 are rare events in live individuals. A combination of the two events in one individual is rarely encountered. Only six live-born cases have so far been reported. Case presentation: Here we reported a case of concomitant UPD(14)mat and mosaic trisomy 14 in a 10-year-old Chinese patient. Most clinical features of our patient were consistent with those previous reported for UPD(14)mat cases, which include prenatal and postnatal growth retardation, neonatal hypotonia, feeding difficulty, intellectual disability, truncal obesity, small hands and feet, short stature, and mild facial dysmorphism, but our patient showed more severe intellectual disability and no sign of precocious puberty. SNP array analysis revealed a mixture of chromosome 14 maternal isodisomy with heterodisomy and a low level trisomy mosaicism of whole chromsome 14 in blood and hyperpigmented skin samples, whereas only UPD(14)mat was detected in normal skin sample. Cytogenetic analysis identified one trisomy 14 cell in 100 metaphase of peripheral blood lymphocytes (47,XX, +14[1]/46,XX[99]). Conclusions: To our knowledge, this is the first case of a patient with UPD(14)mat and mosaic trisomy 14 reported in a Chinese patient. The definitive genetic diagnosis is beneficial for genetic counseling and clinical management of our patient, and for improving our understanding of the genotype-phenotype correlations of concomitant UPD(14)mat and mosaic trisomy 14. Electronic supplementary material The online version of this article (doi:10.1186/s13039-016-0274-4) contains supplementary material, which is available to authorized users.
Published Version: doi:10.1186/s13039-016-0274-4
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4995659/pdf/
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Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:29002594
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