Fig. 1
From: A multicenter study on quality of life of the “greater patient” in congenital ichthyoses
A 2-year-old female with lamellar ichthyosis due to TGM1 mutation shows typical diffuse thick brownish adherent scales (a); a 3-year-old male with congenital ichthyosiform erythroderma due to ABCA12 mutation presents generalized erythroderma with fine whitish scales (b)