Sustained endocrine profiles of a girl with WAGR syndrome

BACKGROUND: Wilms tumor, aniridia, genitourinary anomalies and mental retardation (WAGR) syndrome is a rare genetic disorder caused by heterozygous deletions of WT1 and PAX6 at chromosome 11p13. Deletion of BDNF is known eto be associated with hyperphagia and obesity in both humans and animal models...

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Detaylı Bibliyografya
Yayımlandı:BMC Med Genet
Asıl Yazarlar: Takada, Yui, Sakai, Yasunari, Matsushita, Yuki, Ohkubo, Kazuhiro, Koga, Yuhki, Akamine, Satoshi, Torio, Michiko, Ishizaki, Yoshito, Sanefuji, Masafumi, Torisu, Hiroyuki, Shaw, Chad A., Kagami, Masayo, Hara, Toshiro, Ohga, Shouichi
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2017
Konular:
Case Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5654094/
https://ncbi.nlm.nih.gov/pubmed/29061165
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-017-0477-5
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