Hereditary coproporphyria is a type of porphyria and a rare autosomal dominant genetic disease. It is caused by a deficiency of coproporphyrinogen oxidase, with the main feature being the excretion of large amounts of coproporphyrin III in the feces. The penetrance of this disease is low, and most are asymptomatic gene carriers.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
This section is being translated and completed.
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This information is for health education only and is not a diagnosis. Please consult a qualified clinician if you feel unwell.