Lamellar ichthyosis
Definition
Lamellar ichthyosis is a rare skin condition that affects newborns.
Overview, Causes, & Risk Factors ...
Lamellar ichthyosis
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What is lamellar ichthyosis?
Lamellar ichthyosis is a condition that mainly affects the skin. Infants with this condition are typically born with a tight, clear sheath covering their skin called a collodion membrane.
Lamellar ichthyosis. This severe form of the disease is present at birth and lasts throughout life. Infants with lamellar ichthyosis are born encased in a filmy membrane that's shed after 10 to 14 days, revealing skin that's covered in scales.
Lamellar ichthyosis
Inherited as an autosomal recessive trait, lamellar ichthyosis manifests as retained keratin in large brown scales that lift at the periphery.
When the face is involved, ectropion may be evident.
Lamellar ichthyosis is a rare genetic skin disorder. In lamellar ichthyosis, the skin cells are produced at a normal rate, ...
Lamellar ichthyosis
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Identification and characterization of a novel ABCA subfamily member, ABCA12, located in the lamellar ichthyosis region on 2q34. Cytogenet Genome Res. 2002;98(2-3):169-76. PubMed citation
Hovnanian A.
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 See also: Ichthyosis, Symptom, Deficiency, Dystrophy, Allergy
  
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