Porphyria Cutanea Tarda

"Porphyria Cutanea Tarda" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.
MeSH information
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.


Publications
This graph shows the total number of publications written about "Porphyria Cutanea Tarda" by people in this website by year, and whether "Porphyria Cutanea Tarda" was a major or minor topic of these publications.
Bar chart showing 6 publications over 3 distinct years, with a maximum of 4 publications in 2017
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