Question:
D. wants to know what to use for COPROPORPHYRIA
Answer:
Coproporphyria is a rare genetic disorder that belongs to a group of conditions known as porphyrias. Porphyrias are metabolic disorders caused by abnormalities in the heme biosynthesis pathway, which is essential for producing heme, a critical component of hemoglobin (the protein in red blood cells that carries oxygen).
Coproporphyria specifically results from a deficiency in the enzyme coproporphyrinogen oxidase (CPOX), leading to the accumulation of porphyrins and porphyrin precursors in the body.
Use the general category Porphyrias, which includes all Porphyrias, including Coproporphyria.
Porphyrias: 0.12, 0.49, 0.78, 12.5, 43, 122.4, 262.5, 555.34, 692.5, 819.34