Ozempic Ozempic is a brand name for a weekly subcutaneous injection medicine called Semaglutide that is used together with diet and exercise to treat type 2 diabetes in

ALA dehydratase deficiency porphyria ALA dehydratase deficiency porphyria (ADP) also called ALAD deficiency porphyria, delta-aminolevulinate dehydratase deficiency or Doss porphyria is an extremely rare genetic disorder that involve defects

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