AB156. Clinical and laboratory characteristics of Prader-Willi syndrome

BACKGROUND: Prader-Willi syndrome (PWS) is a complex multisystem genetic disorder due the lack of expression of paternally inherited imprinted genes on chromosome 15q11-13. Clinical presentation includes hypotonia, hyperphagia, obesity, hypogonadism, learning difficulty. The article aims to study cl...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Ann Transl Med
Main Authors: Thao, Bui Phuong, Dung, Vu Chi, Khanh, Nguyen Ngoc, Ngoc, Can Thi Bich, Ngoc, Ngo Diem, Nhung, Dinh Thi Hong, Lan, An Thuy, Mai, Nguyen Thi, Dat, Nguyen Phu, Hoan, Nguyen Thi
Formato: Artigo
Idioma:Inglês
Publicado em: AME Publishing Company 2015
Assuntos:
Part 4: Oral/poster
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563441/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB156
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados