[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0

Aggarwal, Shagun and Vineeth, V.S. and Das Bhowmik, A. and Tandon, A. and Kulkarni, A. and Dhanya Lakshmi, N. and Bhattacherjee, Amrita and Dalal, Ashwin (2020) Exome sequencing for perinatal phenotypes: the significance of deep phenotyping. Prenatal Diagnosis, 40 (2). pp. 260-273. ISSN 0197-3851

[img] Text
Prenatal Diagnosis 40 p260.pdf
Restricted to Repository staff only

Download (6Mb) | Request a copy


OBJECTIVE: To ascertain the performance of Exome Sequencing (ES) technology for determining the etiological basis of abnormal perinatal phenotypes and to study the impact of comprehensive phenotyping on variant prioritisation. METHODS: A carefully selected cohort of 32/204 fetuses with abnormal perinatal phenotypes following post-mortem/postnatal deep phenotyping underwent ESto identify a causative variant for the fetal phenotype. A retrospective comparative analysis of the prenatal versus post-mortem/postnatal phenotype based variant prioritization was performed with aid of Phenolyzer software. A review of selected literature reports was done to examine the completeness of phenotypic information for cases in those reports and how it impacted the performance of fetal ES. RESULTS: In 18/32(56%) fetuses, a pathogenic/likely pathogenic variant was identified. This included novel genotype-phenotype associations, expanded prenatal phenotypes of known Mendelian disorders and dual Mendelian diagnoses. The retrospective analysis revealed that the putative diagnostic variant could not be identified on basis of prenatal findings alone in 15/22(68%) cases, indicating the importance of comprehensive post-mortem/postnatal phenotype information. Literature review was supportive of these findings but could not be conclusive due to marked heterogeneity of involved studies. CONCLUSION: Comprehensive phenotyping is essential for improving diagnostic performance and facilitating identification of novel genotype-phenotype associations in perinatal cohorts undergoing ES.

Item Type: Article
Subjects: Genetics
Depositing User: Dr P Divakar
Date Deposited: 26 Nov 2019 06:10
Last Modified: 07 Feb 2020 06:04
URI: http://cdfd.sciencecentral.in/id/eprint/932

Actions (login required)

View Item View Item