: MeSH: Porphyria Cutanea Tarda

Nutritional and Metabolic Diseases > Metabolic Diseases > Porphyrias > Porphyrias, Hepatic > Porphyria Cutanea Tarda

Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Skin Diseases, Genetic > Porphyrias, Hepatic > Porphyria Cutanea Tarda

Skin and Connective Tissue Diseases > Skin Diseases > Skin Diseases, Genetic > Porphyrias, Hepatic > Porphyria Cutanea Tarda

Digestive System Diseases > Liver Diseases > Porphyrias, Hepatic > Porphyria Cutanea Tarda

Porphyria Cutanea Tarda

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

An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form.

http://data.loterre.fr/ark:/67375/JVR-T78QWMD9-J

RDF/XML TURTLE JSON-LD Creado 22/5/92, última modificación 30/6/18

Loterre