A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2012-03

AUTHORS

Stefan White, Jacqueline Hewitt, Erin Turbitt, Yvonne van der Zwan, Remko Hersmus, Stenvert Drop, Peter Koopman, Vincent Harley, Martine Cools, Leendert Looijenga, Andrew Sinclair

ABSTRACT

Disorders of sex development (DSD) are congenital conditions where chromosomal, gonad or genital development is atypical. In a significant proportion of 46,XY DSD cases it is not possible to identify a causative mutation, making genetic counseling difficult and potentially hindering optimal treatment. Here, we describe the analysis of a 46,XY DSD patient that presented at birth with ambiguous genitalia. Histological analysis of the surgically removed gonads showed bilateral undifferentiated gonadal tissue and immature testis, both containing malignant germ cells. We screened genomic DNA from this patient for deletions and duplications using an Illumina whole-genome SNP microarray. This analysis revealed a heterozygous deletion within the WWOX gene on chromosome 16, removing exons 6-8. Analysis of parental DNA showed that the deletion was inherited from the mother. cDNA analysis confirmed that the deletion maintained the reading frame, with exon 5 being spliced directly onto exon 9. This deletion is the first description of a germline rearrangement affecting the coding sequence of WWOX in humans. Previously described Wwox knockout mouse models showed gonadal abnormalities, supporting a role for WWOX in human gonad development. More... »

PAGES

ejhg2011204

References to SciGraph publications

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URI

http://scigraph.springernature.com/pub.10.1038/ejhg.2011.204

DOI

http://dx.doi.org/10.1038/ejhg.2011.204

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https://app.dimensions.ai/details/publication/pub.1002845762

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/22071891


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