A twin sibling with Prader-Willi syndrome caused by type 2 microdeletion following assisted reproductive technology: A case report

Prader-Willi syndrome (PWS) is a neurobehavioral imprinting disorder, which arises due to an absence of paternally expressed genes within the 15q11.2-q13 region. This occurs via one of the three main genetic mechanisms, as follows: Deletion of the paternally inherited 15q11.2-q13 region, maternal un...

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Detalles Bibliográficos
Autores principales: HAN, JI YOON, PARK, JOONHONG, JANG, WOORI, CHAE, HYOJIN, KIM, MYUNGSHIN, KIM, YONGGOO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906703/
https://www.ncbi.nlm.nih.gov/pubmed/27330749
http://dx.doi.org/10.3892/br.2016.675

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4906703/
https://www.ncbi.nlm.nih.gov/pubmed/27330749
http://dx.doi.org/10.3892/br.2016.675

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