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Among these are classic disorders such as Angelman syndrome and\n                      <jats:italic>MECP2<\/jats:italic>\n                      \u2010related disorder (formerly Rett syndrome), as well as more recently described clinical entities associated with mutations in\n                      <jats:italic>CASK<\/jats:italic>\n                      ,\n                      <jats:italic>CDKL5<\/jats:italic>\n                      ,\n                      <jats:italic>CREBBP<\/jats:italic>\n                      , and\n                      <jats:italic>EP300<\/jats:italic>\n                      (Rubinstein\u2013Taybi syndrome),\n                      <jats:italic>FOXG1<\/jats:italic>\n                      ,\n                      <jats:italic>SLC9A6<\/jats:italic>\n                      (Christianson syndrome), and\n                      <jats:italic>TCF4<\/jats:italic>\n                      (Pitt\u2013Hopkins syndrome). These disorders can be identified clinically by phenotyping across multiple neurodevelopmental and neurobehavioral realms, and enough data are available to recognize these postnatal microcephaly disorders as separate diagnostic entities in their own right. A second diagnostic grouping, comprised of Warburg MICRO syndrome, Cockayne syndrome, and Cerebral\u2010oculo\u2010facial skeletal syndrome, share similar features of somatic growth failure, ophthalmologic, and dysmorphologic features. Many postnatal microcephaly syndromes are caused by mutations in genes important in the regulation of gene expression in the developing forebrain and hindbrain, although important synaptic structural genes also play a role. This is an emerging group of disorders with a fascinating combination of brain malformations, specific epilepsies, movement disorders, and other complex neurobehavioral abnormalities. \u00a9 2014 Wiley Periodicals, Inc.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/ajmg.c.31400","type":"journal-article","created":{"date-parts":[[2014,5,16]],"date-time":"2014-05-16T13:27:17Z","timestamp":1400246837000},"page":"140-155","source":"Crossref","is-referenced-by-count":78,"title":["Genetic disorders associated with postnatal microcephaly"],"prefix":"10.1002","volume":"166","author":[{"given":"Laurie E.","family":"Seltzer","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alex 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