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GTR Home > Conditions/Phenotypes > Ichthyosis with erythrokeratoderma

Ichthyosis with erythrokeratoderma

Summary

Ichthyosis with erythrokeratoderma (IEKD) is an autosomal dominant disorder of cornification characterized by abnormal desquamation in addition to erythematous hyperkeratotic plaques or patches. Lesions are present at birth or appear soon after (Gong et al., 2023; Takeichi et al., 2023). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: IEKD, PRSS20, TLSP, KLK11
    Summary: kallikrein related peptidase 11

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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