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Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome

Known as: WAGR SYNDROME WITH OBESITY, WAGRO, Chromosome 11p13-P12 Deletion Syndrome 
A sub-phenotype of WAGR that includes obesity, and is associated with mutation(s) in the BDNF gene.(NICHD)
National Institutes of Health

Papers overview

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2020
2020
Aniridic fibrosis syndrome was first described by Tsai et al. in 2005. It is a rare complication of invasive intraocular surgery… 
2019
2019
Aniridia is a congenital eye disorder with a variable degree of hypoplasia or absence of iris tissue. It is caused by loss of… 
2015
2015
Congenital aniridia manifests in different forms: it can be transmitted in an autosomal dominant way, as sporadic aniridia, and… 
2015
2015
Congenital aniridia manifests in different forms: it can be transmitted in an autosomal dominant way, as sporadic aniridia, and… 
2014
2014
ZusammenfassungHintergrundDie kongenitale Aniridie tritt in mehreren Formen auf: dominante Vererbung, sporadisch auftretend, als… 
2006
2006
Aniridia usually occurs in isolation, but may also occur as part of the WAGR contiguous gene deletion syndrome, which includes… 
2005
2005
Aniridia, Wilms tumor, genitourinary abnormalities, growth and mental retardation are the cardinal features of the WAGR 11p13…