1. Ashwal S, Michelson D, Plawner L, Dobyns WB; Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Practice parameter: Evaluation… Click to show full abstract
1. Ashwal S, Michelson D, Plawner L, Dobyns WB; Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Practice parameter: Evaluation of the child with microcephaly (an evidence based review): Report of the quality standards subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology 73;2009:887-96. 2. Woods CG. Human microcephaly. Curr Opin Neurobiol 2004;14:112-7. 3. Woods CG, Bond J, Enrad W. Autosomal recessive primary microcephaly: A review of clinical, molecular and evolutionary findings. Am J Hum Genet 2005;76:717-28. 4. Mahmood S, Ahmad W, Hassan MJ. Autosomal recessive primary microcephaly (MCPH): Clinical manifestations, genetic heterogeneity and mutation continuum. Orphanet J Rare Dis 2011;6:39. 5. Cherkaoui Jaouad I, Zrhidri A, Jdioui W, Lyahyai J, Raymond L, Egéa G, et al. A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: A case report. BMC Med Genet 2018;19:118. 6. Nardello R, Fontana A, Antona V, Beninati A, Mangano GD, Stallone MC, et al. A novel mutation of WDR62 gene associated with severe phenotype including infantile spasm, microcephaly and intellectual disability. Brain Dev 2018;40:58-64. 7. Hrachovy RA, Frost JD Jr. Infantile spasms. Cleve Clin J Med 1989;56(Suppl Pt 1):S10-6; discussion S40-2. 8. Iype M, Kunju PA, Saradakutty G, Mohan D, Khan SA. The early electroclinical manifestations of infantile spasms: A video EEG study. Ann Indian Acad Neurol 2016;19:52-7. 9. Naseer MI, Rasool M, Sogaty S, Chaudhary RA, Mansour HM, Chaudhary AG, et al. A novel WDR62 mutation causes primary microcephaly in a large consanguineous Saudi family. Ann Saudi Med 2017;37:148-53.
               
Click one of the above tabs to view related content.