Lamellar ichthyosis is a rare skin condition. It appears at birth and continues throughout life.
Causes, incidence, and risk factors
Lamellar ichthyosis is passed down through families (inherited). Both parents must have at least one abnormal gene to pass the condition to their children.
A baby with this condition is born with a shiny, waxy layer of skin called a collodian membrane. The membrane sheds within the first 2 weeks of life. The underneath is red as scaly skin remains underneath. It resembles the surface of a fish.
Moisturizers containing medicines such as urea, ammonium lactate, or other alpha-hydroxy acids may help shed dead skin layers. Also, retinoid medications such as tazarotene may be applied to the skin.
Babies are at risk for infection when the collodian membrane is shed.
Eye problems may occur later in life because the eyes cannot close completely.