A Japanese patient with a 2p25.3 terminal deletion presented with early‐onset obesity, intellectual disability and diabetes mellitus: A case report

2p25.3 deletion syndrome is a rare genetic disorder that accompanies various phenotypic features, including early‐onset obesity and intellectual disability. Here, we report the first Japanese case of this deletion associated with severe obesity and diabetes mellitus. Microarray‐based comparative gen...

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Detalles Bibliográficos
Autores principales: Sakaue, Taka‐aki, Obata, Yoshinari, Fujishima, Yuya, Kozawa, Junji, Otsuki, Michio, Yamamoto, Toshiyuki, Maeda, Norikazu, Nishizawa, Hitoshi, Shimomura, Iichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847130/
https://www.ncbi.nlm.nih.gov/pubmed/34382350
http://dx.doi.org/10.1111/jdi.13645

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8847130/
https://www.ncbi.nlm.nih.gov/pubmed/34382350
http://dx.doi.org/10.1111/jdi.13645

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