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...

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Dades bibliogràfiques
Publicat a:Ann Transl Med
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: AME Publishing Company 2015
Matèries:
Part 4: Oral/poster
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC4563441/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2305-5839.2015.AB156
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