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• W2118058713 abstract "Genomic microarrays have been used as the first-tier cytogenetic diagnostic test for patients with developmental delay/intellectual disability, autism spectrum disorders and/or multiple congenital anomalies. The use of SNP arrays has revealed regions of homozygosity in the genome which can lead to identification of uniparental disomy and parental consanguinity in addition to copy number variations. Consanguinity is associated with an increased risk of birth defects and autosomal recessive disorders. However, the frequency of parental consanguinity in children with developmental disabilities is unknown, and consanguineous couples may not be identified during doctor’s visit or genetic counseling without microarray. We studied 607 proband pediatric patients referred for developmental disorders using a 4 × 180 K array containing both CGH and SNP probes. Using 720, 360, 180, and 90 Mb as the expected sizes of homozygosity for an estimated coefficient of inbreeding (F) 1/4, 1/8, 1/16, 1/32, parental consanguinity was detected in 21cases (3.46%). Parental consanguinity is not uncommon in children with developmental problems in our study population, and can be identified by use of a combined CGH and SNP chromosome microarray. Identification of parental consanguinity in such cases can be important for further diagnostic testing." @default.
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• W2118058713 date "2013-01-01" @default.
• W2118058713 modified "2023-10-13" @default.
• W2118058713 title "Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray" @default.
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• W2118058713 doi "https://doi.org/10.1186/1755-8166-6-38" @default.
• W2118058713 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3853444" @default.
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