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Porphyria cutanea tarda, familial type

Porphyria cutanea tarda, familial type: Introduction

Porphyria cutanea tarda, familial type: A rare metabolic condition involving a deficiency of the enzyme uroporphyrinogen decarboxylase. More detailed information about the symptoms, causes, and treatments of Porphyria cutanea tarda, familial type is available below.

Symptoms of Porphyria cutanea tarda, familial type

Home Diagnostic Testing

Home medical testing related to Porphyria cutanea tarda, familial type:

Wrongly Diagnosed with Porphyria cutanea tarda, familial type?

Causes of Porphyria cutanea tarda, familial type

Read more about causes of Porphyria cutanea tarda, familial type.

Disease Topics Related To Porphyria cutanea tarda, familial type

Research the causes of these diseases that are similar to, or related to, Porphyria cutanea tarda, familial type:

Misdiagnosis and Porphyria cutanea tarda, familial type

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Porphyria cutanea tarda, familial type: Research Doctors & Specialists

Research related physicians and medical specialists:

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Porphyria cutanea tarda, familial type: Animations

Prognosis for Porphyria cutanea tarda, familial type

Prognosis for Porphyria cutanea tarda, familial type: occasional remission, especially with therapy but cirrhosis may be a problem

Statistics for Porphyria cutanea tarda, familial type

Porphyria cutanea tarda, familial type: Broader Related Topics

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Related Porphyria cutanea tarda, familial type Info

More information about Porphyria cutanea tarda, familial type

  1. Porphyria cutanea tarda, familial type: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Prognosis
 

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