Lamellar Ichthyosis Baby
Keratitis ichthyosis and deafness syndrome.
Lamellar ichthyosis baby. Lamellar ichthyosis also known as ichthyosis lamellaris and nonbullous congenital ichthyosis is a rare inherited skin disorder affecting around 1 in 600000 people. The ichthyosis support group isg was formed in 1997 by a group of individuals affected by ichthyosis to create a network of parents sufferers and. Ichthyosis congenital autosomal recessive 1 with bathing suit distribution collodion baby self healing. Shcb ichthyosis congenita lamellar exfoliation of newborn.
Harlequin type ichthyosis is a genetic disorder which results in thickened skin over nearly the entire body at birth. The skin forms large diamond shaped plates that. Children with some forms of ichthyosis are born covered in a collodion membrane. A tight shiny shell of skin that resembles plastic wrap.
Bilateral contact lens keratitis unresolved. Contact lens keratitis unresolved.
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