Mar. 22, 2022
Nearly 3,000 illustrations, including video clips of neurologic disorders.
Every article is reviewed by our esteemed Editorial Board for accuracy and currency.
Full spectrum of neurology in 1,200 comprehensive articles.
Axial T1-weighted (left) and T2-weighted (right) MRI images of a 6-year-old child with the PEHO phenotype caused by CCDC88A truncating mutation demonstrating reduced brain volume with bilateral, severe pachygyria/lissencephaly. (Source: Nahorski MS, Asai M, Wakeling E, et al. CCDC88A mutations cause PEHO-like syndrome in humans and mouse. Brain 2016;139(Pt 4):1036-44. Creative Commons Attribution License.)