Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome (pronunciation: ker-uh-TOH-sis lin-ee-AIR-is with ik-thee-OH-sis kuhn-JEN-i-tuh and skler-OH-sing ker-uh-TOH-der-muh SIN-drome), often abbreviated as KLICK syndrome, is a rare genetic skin disorder.
Etymology
The term Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome is derived from the Greek words 'keras' (horn), 'ichthys' (fish), and 'scleros' (hard), referring to the characteristic skin abnormalities seen in this condition.
Definition
KLICK syndrome is characterized by three primary symptoms: Keratosis linearis, Ichthyosis congenita, and Sclerosing keratoderma.
- Keratosis linearis refers to the formation of linear, wart-like skin lesions, typically on the extremities.
- Ichthyosis congenita is a condition present at birth that causes the skin to become dry, thick, and scaly.
- Sclerosing keratoderma involves thickening and hardening of the skin on the palms of the hands and soles of the feet.
Related Terms
- Keratosis: A condition marked by an overgrowth of the skin's outermost layer.
- Ichthyosis: A group of skin disorders characterized by dry, scaly, or thickened skin.
- Sclerosing: Referring to the process of hardening or becoming more rigid.
- Keratoderma: A group of conditions characterized by thickening of the skin, usually on the palms and soles.
See Also
- Genetic disorder: A disease caused by abnormalities in an individual's genetic material.
- Skin disorder: A broad term that encompasses various diseases or conditions that affect the skin.
External links
- Medical encyclopedia article on Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
- Wikipedia's article - Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome
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