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Epidermolysis bullosa acquisita

Epidermolysis bullosa acquisita: Introduction

Epidermolysis bullosa acquisita: An acquired autoimmune skin condition characterized by blisters which cause scarring on the skin of joints and sometimes the skull. More detailed information about the symptoms, causes, and treatments of Epidermolysis bullosa acquisita is available below.

Symptoms of Epidermolysis bullosa acquisita

Treatments for Epidermolysis bullosa acquisita

  • Treatment revolves mainly around using medication to suppress the immune system and thus halt the autoimmune process
  • Medication: azathioprine, corticosteroids, colchicines, Dapsone, gold, IV immunoglobulin, mycophenolate mofetil
  • Treat any associated or underlying conditions
  • Minimize physical trauma to the skin
  • If the mouth is involved, the diet should be changed to minimize oral damage i.e. soft food, low acidity foods
  • more treatments...»

Wrongly Diagnosed with Epidermolysis bullosa acquisita?

Epidermolysis bullosa acquisita: Related Patient Stories

Epidermolysis bullosa acquisita: Deaths

Read more about Deaths and Epidermolysis bullosa acquisita.

Epidermolysis bullosa acquisita: Complications

Review possible medical complications related to Epidermolysis bullosa acquisita:

Causes of Epidermolysis bullosa acquisita

Read more about causes of Epidermolysis bullosa acquisita.

Disease Topics Related To Epidermolysis bullosa acquisita

Research the causes of these diseases that are similar to, or related to, Epidermolysis bullosa acquisita:

Misdiagnosis and Epidermolysis bullosa acquisita

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Epidermolysis bullosa acquisita: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Evidence Based Medicine Research for Epidermolysis bullosa acquisita

Medical research articles related to Epidermolysis bullosa acquisita include:

Click here to find more evidence-based articles on the TRIP Database

Epidermolysis bullosa acquisita: Animations

Prognosis for Epidermolysis bullosa acquisita

Prognosis for Epidermolysis bullosa acquisita: The prognosis varies depending on which parts of the body are involved. Mucous membrane involvement tends to cause more problems. The condition usually goes through periods if improvement in symptoms and exacerbation of symptoms.

Research about Epidermolysis bullosa acquisita

Visit our research pages for current research about Epidermolysis bullosa acquisita treatments.

Clinical Trials for Epidermolysis bullosa acquisita

The US based website ClinicalTrials.gov lists information on both federally and privately supported clinical trials using human volunteers.

Some of the clinical trials listed on ClinicalTrials.gov for Epidermolysis bullosa acquisita include:

Epidermolysis bullosa acquisita: Broader Related Topics

User Interactive Forums

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Definitions of Epidermolysis bullosa acquisita:

Form of epidermolysis bullosa characterized by trauma-induced, subepidermal blistering with no family history of the disease. Direct immunofluorescence shows IMMUNOGLOBULIN G deposited at the dermo-epidermal junction. - (Source - Diseases Database)

 

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