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More common in those 30 years or older, but can occur in all age groups.
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Definition for hereditary coproporphyria

Hereditary coproporphyria (HCP) is a form of hepatic porphyria associated with a deficiency of the enzyme coproporphyrinogen III oxidase.


some common symptoms
increased skin sensitivity to sun
rash
stomach pain
tremor


some related diagnoses
1 - 7 of 185 diagnoses
drugs and toxins
trauma
alcoholic hepatitis
toxic hepatitis
lithium poisoning
hepatic failure or coma
liver cirrhosis
  more

do i have 'hereditary coproporphyria'?
In addition the following diagnostic tests might be need to help verify the diagnosis:



therapeutic procedures for 'hereditary coproporphyria'?
Managing or treating a diseases should always be determined by a patients health care provider. Below is a list of associated therapeutic procedures or medications for hereditary coproporphyria:


medications search results for 'hereditary coproporphyria'
1 - 1 of 1 medications
rankings are computer generated. please consult your health care provider.
  Panhematin



web search results for hereditary coproporphyria
Results 1 - 50 - hereditary coproporphyria
en.wikipedia.org - summary
www.ncbi.nlm.nih.gov - summary
www.ncbi.nlm.nih.gov - summary
health.yahoo.com - summary
adam.about.com - summary
ghr.nlm.nih.gov - summary







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MEDgle does not provide medical advice, diagnosis or treatment. Copyright 2006-2012, MEDgle Inc. All Rights Reserved. MEDgle is NOT affiliated with Google. Last Updated: Mar 14, 2012
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