Case Report: Congenital Brain Dysplasia, Developmental Delay and Intellectual Disability in a Patient With a 7q35-7q36.3 Deletion

7q terminal deletion syndrome is a rare condition presenting with multiple congenital malformations, including abnormal brain and facial structures, developmental delay, intellectual disability, abnormal limbs, and sacral anomalies. At least 40 OMIM genes located in the 7q34-7q36.3 region act as can...

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Detalles Bibliográficos
Autores principales: Fan, Liang-Liang, Sheng, Yue, Wang, Chen-Yu, Li, Ya-Li, Liu, Ji-Shi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671813/
https://www.ncbi.nlm.nih.gov/pubmed/34925452
http://dx.doi.org/10.3389/fgene.2021.761003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671813/
https://www.ncbi.nlm.nih.gov/pubmed/34925452
http://dx.doi.org/10.3389/fgene.2021.761003

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