Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome

Keratosis linearis-ichthyosis congenita-sclerosing keratoderma (KLICK) syndrome is an inherited epidermal disorder characterized by palmoplantar keratoderma, linear hyperkeratotic papules on the flexural side of large joints (cord-like distribution around wrists, in antecubital and popliteal folds), hyperkeratotic plaques (on neck, axillae, elbows, wrists, and knees), mild ichthyosiform scaling, and sclerotic constrictions around fingers that present flexural deformities.

Also known as: KLICK syndrome, keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome, KLICK, Klick syndrome, keratosis linearis with ichthyosis congenita and sclerosing keratoderma

0 clinical trials for this condition and its sub-types, 0 tagged with Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome itself.