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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| Hauptverfasser: | , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Wiley
2020-01-01
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| Schriftenreihe: | Case Reports in Pediatrics |
| Online-Zugang: | http://dx.doi.org/10.1155/2020/2031701 |
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