Lamellar ichthyosis: A very rare disorder where an infant is born covered with a transparent membrane which sheds to reveal red scaly skin patches of varying sizes. More detailed information about the symptoms, causes, and treatments of Lamellar ichthyosis is available below.
See full list of 15 symptoms of Lamellar ichthyosis
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Visit our research pages for current research about Lamellar ichthyosis treatments.
The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.
Some of the clinical trials listed on ClinicalTrials.gov for Lamellar ichthyosis include:
Read more about Clinical Trials for Lamellar ichthyosis
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A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds within a few weeks. Scaling is generalized and marked with grayish-brown quadrilateral scales, adherent at their centers and free at the edges. In some cases, scales are so thick that they resemble armored plate. - (Source - Diseases Database)
Lamellar ichthyosis is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Lamellar ichthyosis, or a subtype of Lamellar ichthyosis,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Lamellar ichthyosis as a "rare disease".
Source - Orphanet
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