Autosomal Syndromic Ichthyosis

Chanrarin-Dorfman syndrome

  • Beginning: Childhood.
  • Clinical picture: Severe.
  • Syndromic: It does affect other organs.

At the cutaneous level, it is similar to congenital ichthyosiform erythroderma, but at the extracutaneous level it presents other manifestations such as myopathy, fatty liver and, less frequently, mental and developmental delay, deafness, cardiomyopathy and cataracts.