Ichthyosis is the term for severe, persistent problems with dry skin that almost always start in childhood or infancy. Ichthyosis can be genetic inherited or can develop later in life. In a large majority of people with the disease, the cause is related to one or more genetic mutations. Under normal circumstances, the body continuously renews its skin surface, building new skin cells and allowing older cells to be shed from the surface.
Ichthyosis Vulgaris: Causes, Symptoms, and Diagnosis
But how does this condition get diagnosed and treated? Most cases of ichthyosis are hereditary and begin in childhood. In rare instances, adults can acquire the condition as a side effect of certain medications or other medical conditions. Currently, there is no known cure for the condition, but the consistent and regular use of moisturizers and exfoliants are often enough to resolve symptoms. There are more than 20 different types of ichthyosis, but ichthyosis vulgaris is considered the most common form.
Ichthyosis is a skin disease with more than 20 varieties. Ichthyosis vulgaris is the most common and mildest form of ichthyosis. Of those who have some form of ichthyosis, 95 percent have ichthyosis vulgaris. The main feature of ichthyosis vulgaris is dry, thick and scaly skin. The condition can begin in childhood, often in the first year of life.
Back to Health A to Z. There are at least 20 different types of ichthyosis. Some types are inherited at birth and other types are acquired during adulthood. There's no cure for ichthyosis, but a daily skincare routine usually keeps the symptoms mild and manageable. Most people with ichthyosis have inherited a particular faulty gene from their parent.