Porphyria Cutanea Tarda Porphyria Cutanea Tarda (PCT) is the most common of all porphyrias (one of the hepatic porphyrias) and results from a deficiency of the enzyme
Chloroquine Chloroquine also known as chloroquine phosphate or Aralen phosphate, is an aminoquinoline with antimalarial, anti-inflammatory, and potential chemosensitization and radiosensitization activities ((Vincent, M. J., Bergeron,
Hydroxychloroquine Hydroxychloroquine also known as hydroxychloroquine sulfate, Plaquenil or Plaquenil Sulfate, is a derivative of chloroquine, was developed in 1946. Both chloroquine and hydroxychloroquine chemically belongs
Hepatoerythropoietic Porphyria Hepatoerythropoietic porphyria (HEP) also called UROD-related hepatoerythropoietic porphyria is an extremely rare inherited disorder of the heme-biosynthetic pathway known as cutaneous porphyrias caused by mutations
X-Linked Protoporphyria X-Linked Protoporphyria (XLP) also called X-linked dominant protoporphyria or X-linked dominant erythropoietic protoporphyria is an extremely rare genetic disorder of the heme-biosynthetic pathway known
Hemoglobin H disease Hemoglobin H disease also known as Alpha thalassemia intermedia that is caused by deletion of three alpha-globin genes (only one normal alpha gene
Acute intermittent porphyria Acute intermittent porphyria also called "AIP" or Swedish Porphyria is one of the acute porphyrias, which are a group of rare inherited metabolic
What is tyrosinemia Tyrosinemia also called hereditary tyrosinemia, refers to a group of genetic disorders characterized by disruptions in the multistep process that breaks down
Primary biliary cirrhosis Primary biliary cirrhosis is now known as primary biliary cholangitis or PBC is a chronic progressive autoimmune liver disease in which the small bile