Literature DB >> 28383546

Mosaic trisomy 16: what are the obstetric and long-term childhood outcomes?

Teresa N Sparks1,2, Kao Thao1, Mary E Norton1,2.   

Abstract

PURPOSE: To evaluate obstetric and neonatal outcomes as well as long-term neurodevelopmental outcomes and quality of life among prenatally detected cases of mosaic trisomy (MT16) and confined placental mosaicism (CPM) for trisomy 16.
METHODS: We recruited participants for this cross-sectional study through an international registry of families with children diagnosed with MT16 or CPM. Parents were interviewed about expectations based on prenatal counseling as well as about actual perinatal outcomes, congenital anomalies, medical conditions, and school progress. Health-related quality of life (HRQOL) was assessed via the Pediatric Quality of Life Inventory 4.0 Generic Core Scales.
RESULTS: Forty-four families were enrolled, and 68.2% of the children were female. Common complications were gestational hypertension (gHTN) or preeclampsia (38.1%), preterm delivery (PTD; 71.4%), cesarean delivery (CD; 73.8%), birth weight <10th percentile (73.8%), neonatal intensive care unit (NICU) admission (88.1%), and congenital anomalies (59.5%). However, 81.8% of school-aged children were entirely in mainstream classes, and median physical, psychosocial, and total HRQOL scores were high: 90.6 (34.4-100), 86.7 (35-100), and 84.8 (34.8-100), respectively (100 = optimal quality of life).
CONCLUSION: Several obstetric and neonatal complications are common with pregnancies affected by MT16 or CPM. However, the majority of children demonstrate normal neurodevelopmental outcomes and high HRQOL.Genet Med advance online publication 06 April 2017.

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Year:  2017        PMID: 28383546      PMCID: PMC6029708          DOI: 10.1038/gim.2017.23

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  24 in total

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2.  Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal origin.

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Review 3.  Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.

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4.  Severe fetal malformations associated with trisomy 16 confined to the placenta.

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5.  Increased Nuchal Translucency and Early Growth Retardation Related to Confined Placental Mosaicism of Trisomy 16 in a Dichorionic Twin.

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7.  Evidence for imprinting on chromosome 16: the effect of uniparental disomy on the outcome of mosaic trisomy 16 pregnancies.

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8.  Two cases of trisomy 16 mosaicism ascertained postnatally.

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9.  Identification of differentially methylated genes in first-trimester placentas with trisomy 16.

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