Ocular Findings in the 16p11.2 Microdeletion Syndrome: A Case Report and Literature Review

The recurrent 16p11.2 microdeletion is characterized by developmental delays and a wide spectrum of congenital anomalies. It has been well reported that individuals with this ∼593-kb interstitial deletion have an increased susceptibility toward the autism spectrum disorder (ASD). Abnormalities of th...

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Detalles Bibliográficos
Autores principales: Stingl, Cybil S., Jackson-Cook, Colleen, Couser, Natario L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189309/
https://www.ncbi.nlm.nih.gov/pubmed/32373379
http://dx.doi.org/10.1155/2020/2031701

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189309/
https://www.ncbi.nlm.nih.gov/pubmed/32373379
http://dx.doi.org/10.1155/2020/2031701

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