MeSH Browser

MeSH Supplementary: Poikiloderma of Kindler
Unique ID: C536321
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536321
Entry Term(s): Bullous acrokeratotic poikiloderma of kindler and weary; Congenital bullous poikiloderma; Kindler syndrome; Poikiloderma, congenital, with bullae, weary type; Poikiloderma, hereditary acrokeratotic
Heading Mapped to: *Blister; *Epidermolysis Bullosa; *Periodontal Diseases; *Photosensitivity Disorders
Frequency: 86
Note: A hereditary, autosomal recessive form of epidermolysis bullosa.. It is characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling; periodontal disease may also occur. Mutations in the KIND1 gene have been identified. OMIM: 173650
Date of Entry: 2010/08/25
Revision Date: 2015/08/18

Poikiloderma of Kindler MeSH Supplementary Concept Data 2024