Autosomal recessive congenital ichthyosis 1
MONDO:0009441Any autosomal recessive congenital ichthyosis in which the cause of the disease is a mutation in the TGM1 gene.
Also known as: ARCI1, autosomal recessive congenital ichthyosis 1, autosomal recessive congenital ichthyosis type 1, ichthyosis, congenital, autosomal recessive type 1, LI1, collodion baby, self-healing, collodion fetus, collodion foetus
12 clinical trials for this condition and its sub-types.
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Skin deep: european study probes the hidden emotional toll of skin diseases
Knowledge-focused Not yet recruitingThis study looks at how people with skin conditions (like eczema, psoriasis, or skin cancer) manage stress, feel lonely, and bounce back from challenges. Researchers will compare 375 adults with and without skin disease across 15 European countries using questionnaires. The goal …
Phase: NA • Sponsor: University Hospital, Brest • Aim: Knowledge-focused
Last updated Jun 27, 2026 13:06 UTC
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Rare skin disease patients develop even rarer lymphoma – scientists investigate why
Knowledge-focused Not yet recruitingThis study looks at the blood immune cells of 10 adults with a rare inherited skin condition called NIPAL4 ichthyosis. Researchers want to understand why three patients with this skin disease also developed a very rare lymphoma (Sezary syndrome). By describing the normal immune c…
Sponsor: Assistance Publique - Hôpitaux de Paris • Aim: Knowledge-focused
Last updated Jun 27, 2026 11:02 UTC