: MeSH: Porokeratosis

Skin and Connective Tissue Diseases > Skin Diseases > Keratosis > Porokeratosis

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Porokeratosis

Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Porokeratosis

Porokeratosis

Notice: Undefined index: in /var/www/html/model/Concept.php on line 545

A heritable disorder of faulty keratinization characterized by the proliferation of abnormal clones of KERATINOCYTES and lesions showing varying atrophic patches surrounded by an elevated, keratotic border. These keratotic lesions can progress to overt cutaneous neoplasm. Several clinical variants are recognized, including porokeratosis of Mibelli, linear porokeratosis, disseminated superficial actinic porokeratosis, palmoplantar porokeratosis, and punctate porokeratosis. The classical form of porokeratosis with isolated lesions.

http://data.loterre.fr/ark:/67375/JVR-D3WVWSNN-2

RDF/XML TURTLE JSON-LD Creado 22/5/92, última modificación 22/6/15

Loterre