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Poikiloderma of Kindler MeSH Supplementary Concept Data 2024


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
Registry Number
0
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 Preferred
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