Ontology highlight
ABSTRACT:
SUBMITTER: Di Pierro E
PROVIDER: S-EPMC8391404 | biostudies-literature | 2021 Jul
REPOSITORIES: biostudies-literature
Di Pierro Elena E De Canio Michele M Mercadante Rosa R Savino Maria M Granata Francesca F Tavazzi Dario D Nicolli Anna Maria AM Trevisan Andrea A Marchini Stefano S Fustinoni Silvia S
Diagnostics (Basel, Switzerland) 20210726 8
Porphyrias are a group of diseases that are clinically and genetically heterogeneous and originate mostly from inherited dysfunctions of specific enzymes involved in heme biosynthesis. Such dysfunctions result in the excessive production and excretion of the intermediates of the heme biosynthesis pathway in the blood, urine, or feces, and these intermediates are responsible for specific clinical presentations. Porphyrias continue to be underdiagnosed, although laboratory diagnosis based on the m ...[more]