Takane TJM, Álvarez AML, Daza GRE, Blancas MYL

Language: Spanish
References: 20
Page: 83-90
PDF size: 153.54 Kb.

ABSTRACT

Epidermolysis Bullosa (EB) is a group of genetically determined disorders characterized by blistering in the skin and mucosa following slight trauma. They are classified into three types: simplex, juntional and dystrophic. Dystrophic epidermolysis bullosa (DEB) is caused by mutations in the COL 7 Algene that encodes the production of localized Type VII collagen production in the anchoring fibrils of the dermoepidermal junction. Amongst the most notable of its intraoral are: a high risk of dental caries and periodontal disease, dental anomalies (size and shape), microstomia, iatrogenic blistering, chronic erythematous gingivitis, stomatodynia. The case of a six-yea-old female patient with Recessive Dystrophic Epidermolysis Bullosa is presented

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