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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:BMC Med Genet
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2017
Assuntos:
Case Report
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados