Variegate porphyria Variegate porphyria (VP) also known as South African genetic porphyria is a rare genetic disorder that involve defects in heme or ‘haem’ biosynthetic pathway caused by mutations
Hereditary coproporphyria Hereditary coproporphyria (HCP) is a rare inherited form of liver (hepatic) porphyria, that involve defects in heme or ‘haem’ biosynthetic pathway caused by
Athlete's foot Athlete’s foot also known as tinea pedis is a superficial fungal infection of the skin or dermatophytosis of your foot caused by dermatophytes fungi,
Congenital erythropoietic porphyria Congenital erythropoietic porphyria (CEP) also called Gunther’s disease is an extremely rare inherited autosomal recessive disorder that involve defects in heme or ‘haem’ biosynthetic pathway
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