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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Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: AME Publishing Company 2015
Fag:
Part 4: Oral/poster
Online adgang: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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