Harlequin Ichthyosis: Case Report

• Main Authors: Patrícia A. Couto (Author), Marcela C. Pastore (Author), Jessica C. N. Araújo (Author), Cecilya M. Mota (Author), Caroline A. R. Chirano (Author), Valeria K. A. Ferreira (Author), Sidharta Q. Gadelha (Author), Elaine D. Melo (Author), Patricia C. B. de Melo (Author), Luciana M. Santos (Author)
• Format: Book
• Published: Sociedade Portuguesa de Dermatologia e Venereologia, 2019-03-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Harlequin ichthyosis is a rare autosomal recessive congenital disease in which neonates present generalized hyperkeratotic plaques and deep fissures, ectropion, eclabium, malformation of the auricular pavilion and typical facies. Although several complications related to the skin restriction may occ...