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Article

Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin.

The Journal of investigative dermatology - 1 Mar 2011

Israeli Shirli, Zamir Hadas, Sarig Ofer, Bergman Reuven, Sprecher Eli

Abstract excerpt

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Topics

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Share to Diagnosis, Differential
Share to Glycoproteins
Share to Intercellular Signaling Peptides and Proteins
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Pedigree

Share to Polymorphism, Single Nucleotide

Share to Proteinase Inhibitory Proteins, Secretory

Share to Serine Peptidase Inhibitor Kazal-Type 5

Source

Identifiers

PMID: 21191406
DOI: 10.1038/jid.2010.363

Genes

CDSN

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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Inflammatory peeling skin syndrome caused by a mutation in CDSN encoding corneodesmosin.PMID 21191406Read ↗

Inflammatory peeling skin syndrome caused a novel mutation in CDSN.Semantic proximity Read ↗

Increased expression of caspase-1 and interleukin-18 in peeling skin disease, and a novel mutation of corneodesmosin.Semantic proximity Read ↗

Peeling Skin Disorders: A Paradigm for Skin Desquamation.Semantic proximity Read ↗

A novel mutation in CDSN causes peeling skin disease in a patient from Morocco.Semantic proximity Read ↗

Mutations in the CDSN gene cause peeling skin disease and hypotrichosis simplex of the scalp.Semantic proximity Read ↗

Genetic skin diseases related to desmosomes and corneodesmosomes.Semantic proximity Read ↗

Homozygous deletion of six genes including corneodesmosin on chromosome 6p21.3 is associated with generalized peeling skin disease.Semantic proximity Read ↗

Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses.Semantic proximity Read ↗

The evolving genetic landscape of ILVEN: A comprehensive review.Semantic proximity Read ↗

Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin DiseaseSemantic proximity Read ↗

Genetic diseases of the skin: progress and perspectives.Semantic proximity Read ↗

Acral Peeling Skin Syndrome Resulting from a Homozygous Nonsense Mutation in the <i><scp>CSTA</scp></i> Gene Encoding Cystatin ASemantic proximity Read ↗

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