Unusual Presentation in WAGR Syndrome: Expanding the Phenotypic and Genotypic Spectrum of the Diseases
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DOI: 10.3390/genes13081431
Abstract: The deletion of chromosome 11p13 involving the WT1 and PAX6 genes has been shown to cause WAGR syndrome (OMIM #194072), a rare genetic disorder that features Wilms’ tumor, aniridia, genitourinary anomalies, as well as mental… read more here.
Keywords: wagr syndrome; unusual presentation; spectrum; phenotypic ... See more keywords