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Diseases » Brunzell syndrome » Summary
 

What is Brunzell syndrome?

What is Brunzell syndrome?

  • Brunzell syndrome: A rare recessively inherited syndrome characterized by a lack of skin fat (Seip syndrome), cystic angiomatosis of the long bones which can lead to fractures.
  • Brunzell syndrome: An autosomal recessive form of diabetes, characterized by the generalized lipoatrophy.
    Source - Diseases Database

Brunzell syndrome: Introduction

Types of Brunzell syndrome:

Broader types of Brunzell syndrome:

How serious is Brunzell syndrome?

Complications of Brunzell syndrome: see complications of Brunzell syndrome

What causes Brunzell syndrome?

Causes of Brunzell syndrome: see causes of Brunzell syndrome

What are the symptoms of Brunzell syndrome?

Symptoms of Brunzell syndrome: see symptoms of Brunzell syndrome

Complications of Brunzell syndrome: see complications of Brunzell syndrome

Brunzell syndrome: Testing

Misdiagnosis: see misdiagnosis and Brunzell syndrome.

How is it treated?

Doctors and Medical Specialists for Brunzell syndrome: Medical Geneticist ; see also doctors and medical specialists for Brunzell syndrome.
Treatments for Brunzell syndrome: see treatments for Brunzell syndrome
Research for Brunzell syndrome: see research for Brunzell syndrome

Name and Aliases of Brunzell syndrome

Main name of condition: Brunzell syndrome

Other names or spellings for Brunzell syndrome:

Angiomatosis systemic cystic Seip syndrome

Lawrence-Seip syndrome, Lipoatrophic diabetes mellitus, Seip's syndrome, Berardinelli lipodystrophy syndrome Source - Diseases Database

 

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