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What is Franek-Bocker-Kahlen syndrome?

What is Franek-Bocker-Kahlen syndrome?

  • Franek-Bocker-Kahlen syndrome: A rare syndrome characterized mainly by a small head, brain defect, spasticity and high sodium level.

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

Franek-Bocker-Kahlen syndrome: Introduction

What causes Franek-Bocker-Kahlen syndrome?

Causes of Franek-Bocker-Kahlen syndrome: see causes of Franek-Bocker-Kahlen syndrome

What are the symptoms of Franek-Bocker-Kahlen syndrome?

Symptoms of Franek-Bocker-Kahlen syndrome: see symptoms of Franek-Bocker-Kahlen syndrome

Franek-Bocker-Kahlen syndrome: Testing

Diagnostic testing: see tests for Franek-Bocker-Kahlen syndrome.

Misdiagnosis: see misdiagnosis and Franek-Bocker-Kahlen syndrome.

How is it treated?

Treatments for Franek-Bocker-Kahlen syndrome: see treatments for Franek-Bocker-Kahlen syndrome

Name and Aliases of Franek-Bocker-Kahlen syndrome

Main name of condition: Franek-Bocker-Kahlen syndrome

Other names or spellings for Franek-Bocker-Kahlen syndrome:

Microcephaly [brain defect - spasticity - hypernatremia]


 » Next page: Online Medical Textbooks for Franek-Bocker-Kahlen syndrome

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