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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
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A sub-phenotype of WAGR that includes obesity, and is associated with mutation(s) in the BDNF gene.(NICHD)
National Institutes of Health
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Related topics
Related topics
3 relations
Neoplastic Syndromes, Hereditary
Broader (2)
Obesity
WAGR Syndrome
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Aniridic Fibrosis Syndrome
M. Moshirfar
,
Jordan P. Hastings
,
Y. Ronquillo
2020
Corpus ID: 216542529
Aniridic fibrosis syndrome was first described by Tsai et al. in 2005. It is a rare complication of invasive intraocular surgery…
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2019
2019
WAGRO syndrome: a rare genetic condition associated with aniridia and additional ophthalmologic abnormalities.
M. A. T. Ferreira
,
Ivan Gonçalves de Almeida Júnior
,
+5 authors
P. Zen
Arquivos Brasileiros de Oftalmologia
2019
Corpus ID: 162172087
Aniridia is a congenital eye disorder with a variable degree of hypoplasia or absence of iris tissue. It is caused by loss of…
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2015
2015
Aniridia Guides and Aniridia-Syndrome (PAX6-Syndrome): Do’s and Dont’s in Clinical Care
B. Käsmann-Kellner
,
A. Viestenz
,
B. Seitz
2015
Corpus ID: 77717145
Congenital aniridia manifests in different forms: it can be transmitted in an autosomal dominant way, as sporadic aniridia, and…
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2015
2015
Медицинское сопровождение врожденной аниридии и аниридийного синдрома (РАХ6-синдрома)
Б. Касман-келнер
,
А. Вейстенц
,
Б. Зейц
2015
Corpus ID: 196335334
Congenital aniridia manifests in different forms: it can be transmitted in an autosomal dominant way, as sporadic aniridia, and…
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2014
2014
Aniridiesyndrom
B. Käsmann-Kellner
,
B. Seitz
Der Ophthalmologe
2014
Corpus ID: 195676180
ZusammenfassungHintergrundDie kongenitale Aniridie tritt in mehreren Formen auf: dominante Vererbung, sporadisch auftretend, als…
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2013
2013
The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome.
R. Rodríguez-López
,
José M Carbonell Pérez
,
+10 authors
E. G. Gómez
Gene
2013
Corpus ID: 44903452
2006
2006
WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH
P. Lennon
,
D. Scott
,
+4 authors
S. Cheung
American Journal of Medical Genetics. Part A
2006
Corpus ID: 7203481
Aniridia usually occurs in isolation, but may also occur as part of the WAGR contiguous gene deletion syndrome, which includes…
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2006
2006
Clinical, cytogenetic and molecular characterization of a patient with combined succinic semialdehyde dehydrogenase deficiency and incomplete WAGR syndrome with obesity.
R. Jung
,
A. Rauch
,
+9 authors
I. Knerr
Molecular Genetics and Metabolism
2006
Corpus ID: 37413362
2005
2005
Combination of WAGR and Potocki–Shaffer contiguous deletion syndromes in a patient with an 11p11.2–p14 deletion
D. Bremond-Gignac
,
J. Crolla
,
+7 authors
A. Verloes
European Journal of Human Genetics
2005
Corpus ID: 1022756
Aniridia, Wilms tumor, genitourinary abnormalities, growth and mental retardation are the cardinal features of the WAGR 11p13…
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