Possibility of early diagnosis in a fetus affected by Prader-Willi syndrome with maternal hetero-UPD15: A lesson to be learned

Prader-Willi syndrome (PWS), a complicated neurodevelopmental disorder arising from errors in genomic imprinting, is characterized by evident hypotonia along with feeding difficulties and the absence of crying in early infancy. Hyperphagia and obesity are not uncommon in patients with PWS, usually a...

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Detalles Bibliográficos
Autores principales: Dong, Yanling, Liu, Shu, Li, Junnan, Li, Jian, Chen, Qian, Luo, Jianyun, Li, Chunlei, Li, Huifan, Qi, Hongbo, Li, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580037/
https://www.ncbi.nlm.nih.gov/pubmed/31115529
http://dx.doi.org/10.3892/mmr.2019.10246

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6580037/
https://www.ncbi.nlm.nih.gov/pubmed/31115529
http://dx.doi.org/10.3892/mmr.2019.10246

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