MeSH Browser

MeSH Supplementary: Peeling Skin Syndrome
Unique ID: C564818
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564818
Entry Term(s): Deciduous Skin; Keratolysis Exfoliativa Congenita; Peeling skin syndrome 1; Skin Peeling, Familial Continuous Generalized
Heading Mapped to: *Dermatitis, Exfoliative; *Skin Diseases, Genetic
Frequency: 36
Note: A rare, hereditary, autosomal recessive genodermatosis with onset from birth to adulthood. Clinically, it is characterized by spontaneous superficial peeling of the skin with or without PRURITIS, which sometimes is accompanied by ERYTHEMA or vesiculation. The skin involvement is usually general, but in some patients the scalp, face, palms, and soles may be unaffected. Seasonal changes have been reported. Histologically, it is characterized by separation of the EPIDERMIS between the statum corneum and the stratum granulosum. Mutations in the CDSN gene have been identified. OMIM: 270300
Date of Entry: 2012/11/05
Revision Date: 2015/09/27

Concept UI: M0565118
Terms: Peeling Skin Syndrome Preferred Term
Term UI T805673
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Peeling skin syndrome 1
Term UI T000885649
Date08/27/2015
LexicalTag NON
ThesaurusID OMIM (2016); Skin Peeling, Familial Continuous Generalized
Term UI T805674
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Keratolysis Exfoliativa Congenita
Term UI T805675
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Deciduous Skin
Term UI T805676
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

Peeling Skin Syndrome MeSH Supplementary Concept Data 2024