ALLMedicine™ WAGR Syndrome Center

Jan 4th, 2021 - WAGR syndrome.|2021|Shimamura Y,Okamoto T,Abe K,Takuto M,Ogawa Y,|

Dec 10th, 2020 - Introduction: Wilms tumor (WT) is the most common renal malignancy of children and can be seen in WAGR syndrome (WT, aniridia, genitourinary anomalies, and intellectual disability). WAGR results from a contiguous gene deletion within the 11p13 reg...

Nov 4th, 2020 - WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare contiguous gene deletion syndrome with a 45% to 60% risk of developing Wilms tumor (WT). Currently, surveillance and treatment recommendati...

Sep 19th, 2020 - Because of the significant occurrence of "WAGR-region" deletions among de novo mutations detected in congenital aniridia, DNA diagnosis is critical for all sporadic cases of aniridia due to its help in making an early diagnosis of WAGR syndrome. S...

Sep 11th, 2020 - In this study, we present the management of an intra-articular fracture in a 13-year-old boy with WAGR Syndrome, an extremely rare genetic disorder. The goal of this study is to provide possible solutions to the complex pain management requirement...

Jan 4th, 2021 - WAGR syndrome.|2021|Shimamura Y,Okamoto T,Abe K,Takuto M,Ogawa Y,|

Dec 10th, 2020 - Introduction: Wilms tumor (WT) is the most common renal malignancy of children and can be seen in WAGR syndrome (WT, aniridia, genitourinary anomalies, and intellectual disability). WAGR results from a contiguous gene deletion within the 11p13 reg...

Nov 4th, 2020 - WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare contiguous gene deletion syndrome with a 45% to 60% risk of developing Wilms tumor (WT). Currently, surveillance and treatment recommendati...

Sep 19th, 2020 - Because of the significant occurrence of "WAGR-region" deletions among de novo mutations detected in congenital aniridia, DNA diagnosis is critical for all sporadic cases of aniridia due to its help in making an early diagnosis of WAGR syndrome. S...

Sep 11th, 2020 - In this study, we present the management of an intra-articular fracture in a 13-year-old boy with WAGR Syndrome, an extremely rare genetic disorder. The goal of this study is to provide possible solutions to the complex pain management requirement...

Aug 27th, 2008 - Action Points Explain to patients who ask that some individuals may carry genetic variants that make them particularly susceptible to weight gain when exposed to the current Western lifestyle. Explain that as yet there is no pharmacologic answer f...