Autosomal recessive congenital ichthyosis 2

An autosomal recessive condition caused by mutation(s) in the ALOX12B gene, encoding arachidonate 12-lipoxygenase, 12R-type. It is characterized by dry, thickened, scaly skin.

Also known as: ARCI2, autosomal recessive congenital ichthyosis type 2, ichthyosis, congenital, autosomal recessive type 2, NBCIE, NCIE, collodion baby, self-healing, ichthyosiform erythroderma, Brocq congenital, nonbullous form, ichthyosiform erythroderma, Brocq congenital, nonbullous form, formerly

10 clinical trials for this condition and its sub-types.