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erythroderma
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Genetic Markers
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Curated Studies
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Skin biopsies from patients with ichthyosis subtypes
OMIM - Chanarin-Dorfman syndrome
OMIM - Skin Related Disorders
OMIM - Bullous ichthyosiform erythroderma
OMIM - Ichthyosis
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Literature
Most Relevant Literature
Congenital ichthyosiform erythroderma due to a CYP4F22 mutation responds to ustekinumab: A case repo…
Novel homozygous missense mutation c.1654G>T in the ALOX12B gene causing congenital ichthyosiform er…
Cushing disease in a patient with nonbullous congenital ichthyosiform erythroderma: lessons in avoid…
Secukinumab in the treatment of a child with congenital ichthyosiform erythroderma with ABCA12 mutat…
Recessive mosaicism in ABCA12 causes blaschkoid congenital ichthyosiform erythroderma.
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An Open-label, Non-controlled Study of KHK4827 in Subjects With Psoriasis
A Clinical Study of Increased Dose of TA-650 in Patients With Psoriasis
A Phase 3 Clinical Study of KHK 4827
A Phase 4 Clinical Study of Brodalumab
The Efficacy and Safety of Secukinumab in Patients With Ichthyoses
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