Nager Syndrome: Report of Clinical and Radiological Findings in an Egyptian InfantEbtesam Abdalla*
Medical Research Institute, Alexandria, Egypt
- *Corresponding Author:
- Ebtesam Mohamed Abdalla
Medical Research Institute
Human Genetics, Alexandria
E-mail: [email protected]
Received date: Mar 15, 2016 Accepted date: Mar 18, 2016 Published date: Mar 25, 2016
Citation: Abdalla E (2016) Nager Syndrome: Report of Clinical and Radiological Findings in an Egyptian Infant. J Genet Syndr Gene Ther 7:I103. doi:10.4172/2157-7412.1000I103
Copyright: © 2016 Abdalla E, et al., This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Nager syndrome is an extremely rare genetic condition, that this case is the first reported from Egypt. The affected infant manifested a severe phenotype with growth retardation and congenital heart defect. Limb anomalies are a cardinal sign and, in combination with the characteristic craniofacial features, are diagnostic.