Joyce T. Turner's research while affiliated with George Washington University and other places
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Publications (3)
The Oncology Grand Rounds series is designed to place original reports published in the Journal into clinical context. A case presentation is followed by a description of diagnostic and management challenges, a review of the relevant literature, and a summary of the authors' suggested management approaches. The goal of this series is to help reader...
Wilms tumor (WT) is the most common renal tumor in pediatrics, representing 6.3% of all childhood cancers. It is a developmental neoplasm that arises from embryonic kidney precursor cells. Most WTs are sporadic, but about 10–15% of patients have clinical features that suggest the presence of a constitutional predisposing mutation. Such features inc...
WT1‐related disorders are a group of conditions associated with an aberrant or absent copy of the WT1 gene. WT1 encodes a zinc‐finger protein that not only acts as a tumor suppressor, but also is important for gonadal, urogenital tract, and diaphragmatic development. This group of conditions encompasses a phenotypic spectrum that includes WAGR synd...
Citations
... Identified driver genes include WT1, TRIM28, REST, and the 11p15 locus, and they are associated with conditions varying from easily recognisable syndromes to only an increased risk of WT [10]. However, the prevalence of (epi)genetic alterations known to predispose to WT likely represents only the tip of the iceberg [11][12][13], and this consideration takes us to level B of the debate. ...
![[object Object]](https://i1.rgstatic.net/ii/profile.image/288908786061312-1445892630222_Q64/D-Ashley-Hill.jpg)
... Wilms' tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR; OMIM#194072) syndrome is a contiguous gene deletion syndrome caused by a de novo deletion including the 11p13 region [1,2]. Autism spectrum disorder (ASD) is a behaviorally defined neurodevelopmental syndrome associated with various genetic and non-genetic causes [3] that is frequently observed in individuals with WAGR syndrome at a reported incidence of 20-52%, which is markedly higher than in the general population (1-4%) [1,[4][5][6]. ...
