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Epidermolysis bullosa, junctional, Herlitz-Pearson

Epidermolysis bullosa, junctional, Herlitz-Pearson: Introduction

Epidermolysis bullosa, junctional, Herlitz-Pearson: A rare blistering skin disease which can often result in infant death. More detailed information about the symptoms, causes, and treatments of Epidermolysis bullosa, junctional, Herlitz-Pearson is available below.

Symptoms of Epidermolysis bullosa, junctional, Herlitz-Pearson

Wrongly Diagnosed with Epidermolysis bullosa, junctional, Herlitz-Pearson?

Epidermolysis bullosa, junctional, Herlitz-Pearson: Related Patient Stories

Epidermolysis bullosa, junctional, Herlitz-Pearson: Deaths

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Epidermolysis bullosa, junctional, Herlitz-Pearson: Complications

Review possible medical complications related to Epidermolysis bullosa, junctional, Herlitz-Pearson:

Causes of Epidermolysis bullosa, junctional, Herlitz-Pearson

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Disease Topics Related To Epidermolysis bullosa, junctional, Herlitz-Pearson

Research the causes of these diseases that are similar to, or related to, Epidermolysis bullosa, junctional, Herlitz-Pearson:

Misdiagnosis and Epidermolysis bullosa, junctional, Herlitz-Pearson

Psoriasis often undiagnosed cause of skin symptoms in children: Children who suffer from the skin disorder called psoriasis can often go undiagnosed. The main problem is that psoriasis is...read more »

Epidermolysis bullosa, junctional, Herlitz-Pearson: Research Doctors & Specialists

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Epidermolysis bullosa, junctional, Herlitz-Pearson: Animations

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Definitions of Epidermolysis bullosa, junctional, Herlitz-Pearson:

Form of epidermolysis bullosa having onset at birth or during the neonatal period and transmitted through autosomal recessive inheritance. It is characterized by generalized blister formation, extensive denudation, and separation and cleavage of the basal cell plasma membranes from the basement membrane. - (Source - Diseases Database)

Epidermolysis bullosa, junctional, Herlitz-Pearson is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Epidermolysis bullosa, junctional, Herlitz-Pearson, or a subtype of Epidermolysis bullosa, junctional, Herlitz-Pearson, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

 

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