8q22.2q22.3 Microdeletion Syndrome Associated with Hearing Loss and Intractable Epilepsy
8q22.2q22.3 microdeletion syndrome has been described in only seven patients. We present a new case from Colombia. The characteristics of this condition are developmental delay, microcephaly, seizures, and typical facial dysmorphism. We discuss the clinical phenotype of the patient presenting releva...
Main Authors: | Alejandra Rincon, Paola Paez-Rojas, Fernando Suárez-Obando |
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Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2019-01-01
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Series: | Case Reports in Genetics |
Online Access: | http://dx.doi.org/10.1155/2019/7608348 |
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