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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654094/
https://www.ncbi.nlm.nih.gov/pubmed/29061165
http://dx.doi.org/10.1186/s12881-017-0477-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5654094/
https://www.ncbi.nlm.nih.gov/pubmed/29061165
http://dx.doi.org/10.1186/s12881-017-0477-5

Ejemplares similares