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...

Descripción completa

Detalles Bibliográficos
Autores principales: Lukoshe, Akvile, White, Tonya, Schmidt, Marcus N, van der Lugt, Aad, Hokken-Koelega, Anita C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015928/
https://www.ncbi.nlm.nih.gov/pubmed/24144356
http://dx.doi.org/10.1186/1866-1955-5-31

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015928/
https://www.ncbi.nlm.nih.gov/pubmed/24144356
http://dx.doi.org/10.1186/1866-1955-5-31

Ejemplares similares