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What is Burnett-Schwartz-Berberian syndrome?

What is Burnett-Schwartz-Berberian syndrome?

  • Burnett-Schwartz-Berberian syndrome: A rare syndrome characterized by an inflammatory facial skin disorder and various congenital anomalies.

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

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Burnett-Schwartz-Berberian syndrome as a "rare disease".
Source - Orphanet

Burnett-Schwartz-Berberian syndrome: Introduction

Types of Burnett-Schwartz-Berberian syndrome:

Broader types of Burnett-Schwartz-Berberian syndrome:

What causes Burnett-Schwartz-Berberian syndrome?

Causes of Burnett-Schwartz-Berberian syndrome: see causes of Burnett-Schwartz-Berberian syndrome

What are the symptoms of Burnett-Schwartz-Berberian syndrome?

Symptoms of Burnett-Schwartz-Berberian syndrome: see symptoms of Burnett-Schwartz-Berberian syndrome

Burnett-Schwartz-Berberian syndrome: Testing

Diagnostic testing: see tests for Burnett-Schwartz-Berberian syndrome.

Misdiagnosis: see misdiagnosis and Burnett-Schwartz-Berberian syndrome.

How is it treated?

Doctors and Medical Specialists for Burnett-Schwartz-Berberian syndrome: Neonatologist ; see also doctors and medical specialists for Burnett-Schwartz-Berberian syndrome.
Treatments for Burnett-Schwartz-Berberian syndrome: see treatments for Burnett-Schwartz-Berberian syndrome

Name and Aliases of Burnett-Schwartz-Berberian syndrome

Main name of condition: Burnett-Schwartz-Berberian syndrome

Other names or spellings for Burnett-Schwartz-Berberian syndrome:

Ulerythema ophryogenesis (subtype), Ulerythema ophryogenesis with multiple congenital anomalies, Ulerythema ophryogenes with multiple congenital anomalies, Keratosis Pilaris Atrophicans Facies, Ulerythema ophryogenes, Keratosis pilaris

Keratosis Pilaris Atrophicans Facies, Keratosis pilaris, Ulerythema ophryogenes, Ulerythema ophryogenes with multiple congenital anomalies
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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