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- W2739145092 abstract "Maternal uniparental disomy (UPD) 15 is one of the molecular causes of Prader-Willi syndrome (PWS), a multisystem disorder which presents with neonatal hypotonia and feeding difficulty. Current diagnostic algorithms differ regarding the use of SNP microarray to detect PWS. We retrospectively examined the frequency with which SNP microarray could identify regions of homozygosity (ROH) in patients with PWS. We determined that 7/12 (58%) patients with previously confirmed PWS by methylation analysis and microsatellite-positive UPD studies had ROH (>10 Mb) by SNP microarray. Additional assessment of 5,000 clinical microarrays, performed from 2013 to present, determined that only a single case of ROH for chromosome 15 was not caused by an imprinting disorder or identity by descent. We observed that ROH for chromosome 15 is rarely incidental and strongly associated with hypotonic infants having features of PWS. Although UPD microsatellite studies remain essential to definitively establish the presence of UPD, SNP microarray has important utility in the timely diagnostic algorithm for PWS." @default.
- W2739145092 created "2017-07-31" @default.
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- W2739145092 date "2017-01-01" @default.
- W2739145092 modified "2023-09-25" @default.
- W2739145092 title "Assessing the Clinical Utility of SNP Microarray for Prader-Willi Syndrome due to Uniparental Disomy" @default.
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- W2739145092 doi "https://doi.org/10.1159/000478921" @default.
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