From: Ichthyosis: case report in a Colombian man with genetic alterations in ABCA12 and HRNR genes
Phenotypes | Associated genes |
---|---|
Common ichthyosis | |
Ichthyosis vulgaris | FLG, HRNR |
Recessive X-linked ichthyosis | STS, VCX3A |
Autosomal recessive congenital ichthyosis | |
Major types | |
Harlequin ichthyosis | ABCA12 |
Lamellar ichthyosis | ABCA12, ALOXE3, ALOX12B, CERS3, CYP4F22, NIPAL4/ICHTHYIN, PNPLA1, TGM1 |
Congenital ichthyosiform erythroderma | ABCA12, ALOXE3, ALOX12B, CERS3, CYP4F22, LIPN, NIPAL4/ICHTHYIN, PNPLA1, TGM1 |
Minor types | |
Self-healing collodion baby | ALOXE3, ALOX12B, TGM1 |
Acral self-healing collodion baby | TGM1 |
Bathing suit ichthyosis | TGM1 |