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CERS3-nEDD

Previously: Lamellar ichthyosis, CIE, ARCI

nEDD Gene: CERS3 AR

Onset: Birth

Pathway: Lipid synthesis and transport

Category Paper: nEDD Paper

CERS3-nEDD: erythroderma with minimal scaling.

Key Clinical Clues

Collodion membrane at birth, generalized fine scales and erythroderma.

References

Radner FPW, Marrakchi S, Kirchmeier P et al. Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans. PLOS Genet 2013; 9:e1003536.

Summarised from published literature for general information. This is not medical advice, and entries are still being verified. Read the full disclaimer