Incidental Finding of MEGDEL Syndrome at a Tertiary Care Center in Saudi Arabia
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Publisher
Springer Science and Business Media LLC
Reference8 articles.
1. MEGDEL syndrome;Finsterer J;Pediatr Neurol,2020
2. Two Turkish siblings with MEGDEL syndrome due to novel SERAC1 gene mutation;Ünal Ö;Turk J Pediatr,2015
3. Incidental finding of MEGDEL syndrome based on neuroimaging: case report;Alshammari SA;Case Rep Neurol,2021
4. Adult-onset generalized dystonia as the main manifestation of MEGDEL syndrome;Giron C;Tremor Other Hyperkinet Mov (N Y),2018
5. A novel mutation in the SERAC1 gene correlates with the severe manifestation of the MEGDEL phenotype, as revealed by whole-exome sequencing;Alagoz M;Exp Ther Med,2020
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