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What is Nyssen-Van Bogaert syndrome?

What is Nyssen-Van Bogaert syndrome?

  • Nyssen-Van Bogaert syndrome: An adult form of an inherited biochemical disorder involving a deficiency of an enzyme called cerebroside sulfatase. The enzyme deficiency causes cerebroside sulfate to build up within the body and causes damage to the nervous system including the brain.

Nyssen-Van Bogaert syndrome: Introduction

Types of Nyssen-Van Bogaert syndrome:

Broader types of Nyssen-Van Bogaert syndrome:

What causes Nyssen-Van Bogaert syndrome?

Causes of Nyssen-Van Bogaert syndrome: see causes of Nyssen-Van Bogaert syndrome

What are the symptoms of Nyssen-Van Bogaert syndrome?

Symptoms of Nyssen-Van Bogaert syndrome: see symptoms of Nyssen-Van Bogaert syndrome

Onset of Nyssen-Van Bogaert syndrome: usually after puberty

Nyssen-Van Bogaert syndrome: Testing

Diagnostic testing: see tests for Nyssen-Van Bogaert syndrome.

Misdiagnosis: see misdiagnosis and Nyssen-Van Bogaert syndrome.

How is it treated?

Doctors and Medical Specialists for Nyssen-Van Bogaert syndrome: Medical Geneticist ; see also doctors and medical specialists for Nyssen-Van Bogaert syndrome.
Treatments for Nyssen-Van Bogaert syndrome: see treatments for Nyssen-Van Bogaert syndrome

Name and Aliases of Nyssen-Van Bogaert syndrome

Main name of condition: Nyssen-Van Bogaert syndrome

Other names or spellings for Nyssen-Van Bogaert syndrome:

Van Bogaert-Nyssen-Pfeiffer syndrome

 

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