Sign Up for a Free Account

This is an image preview.
Start a Free Account
to view the full image.

  • 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.

  • Listen to MedLink on the go with Audio versions of each article.

PEHO: characteristic facies

Characteristic facies with swollen cheeks, narrow sloping forehead, and microcephaly in a 6-year-old child with the PEHO phenotype caused by CCDC88A truncating mutation. (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.)

Related Article

Related Media

Associated Disorders

  • Infantile spasms
  • Lennox-Gastaut syndrome