Divergent structural brain abnormalities between different genetic subtypes of children with Prader–Willi syndrome

BACKGROUND: Prader–Willi syndrome (PWS) is a complex neurogenetic disorder with symptoms that indicate not only hypothalamic, but also a global, central nervous system (CNS) dysfunction. However, little is known about developmental differences in brain structure in children with PWS. Thus, our aim w...

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Detaylı Bibliyografya
Asıl Yazarlar: Lukoshe, Akvile, White, Tonya, Schmidt, Marcus N, van der Lugt, Aad, Hokken-Koelega, Anita C
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2013
Konular:
Research
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4015928/
https://ncbi.nlm.nih.gov/pubmed/24144356
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1866-1955-5-31
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