Editing Microcephaly (section)

===Microlissencephaly===
{{Main|Microlissencephaly}}
[[Microlissencephaly]] is microcephaly combined with [[lissencephaly]] (smooth brain surface due to absent [[Sulcus (neuroanatomy)|sulci]] and [[gyri]]). Most cases of microlissencephaly are described in consanguineous families, suggesting an [[autosomal recessive inheritance]].<ref name="Cavallin">{{Cite journal|last1=Cavallin|first1=Mara|last2=Rujano|first2=Maria A.|last3=Bednarek|first3=Nathalie|last4=Medina-Cano|first4=Daniel|last5=Bernabe Gelot|first5=Antoinette|last6=Drunat|first6=Severine|last7=Maillard|first7=Camille|last8=Garfa-Traore|first8=Meriem|last9=Bole|first9=Christine|date=2017-10-01|title=WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells|journal=Brain|volume=140|issue=10|pages=2597–2609|doi=10.1093/brain/awx218|issn=1460-2156|pmid=28969387|doi-access=free}}</ref><ref>{{Cite book|url={{GBUrl|AmZgmGG4Dz0C|pg=PA309}}|title=Caffey's Pediatric Diagnostic Imaging E-Book|last=Coley|first=Brian D.|date=2013 |publisher=Elsevier Health Sciences|isbn=978-1-4557-5360-4 |edition=12th |oclc=847214216}}</ref><ref>{{Cite book|url={{GBUrl|AnVYBAAAQBAJ|pg=PA838}}|title=Fanaroff and Martin's Neonatal-Perinatal Medicine E-Book: Diseases of the Fetus and Infant|last1=Martin|first1=Richard J.|last2=Fanaroff|first2=Avroy A.|last3=Walsh|first3=Michele C.|date=2014 |publisher=Elsevier Health Sciences|isbn=978-0-323-29537-6 |oclc=909892605}}</ref>