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What is Bosma-Henkin-Christiansen syndrome?

What is Bosma-Henkin-Christiansen syndrome?

  • Bosma-Henkin-Christiansen syndrome: A rare syndrome characterized mainly by a reduced sense of smell, an underdeveloped nose and hypogonadism.

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

Bosma-Henkin-Christiansen syndrome: Introduction

Types of Bosma-Henkin-Christiansen syndrome:

Broader types of Bosma-Henkin-Christiansen syndrome:

What causes Bosma-Henkin-Christiansen syndrome?

Causes of Bosma-Henkin-Christiansen syndrome: see causes of Bosma-Henkin-Christiansen syndrome

What are the symptoms of Bosma-Henkin-Christiansen syndrome?

Symptoms of Bosma-Henkin-Christiansen syndrome: see symptoms of Bosma-Henkin-Christiansen syndrome

Bosma-Henkin-Christiansen syndrome: Testing

Diagnostic testing: see tests for Bosma-Henkin-Christiansen syndrome.

Misdiagnosis: see misdiagnosis and Bosma-Henkin-Christiansen syndrome.

How is it treated?

Doctors and Medical Specialists for Bosma-Henkin-Christiansen syndrome: Otolaryngologist, Neurologist ; see also doctors and medical specialists for Bosma-Henkin-Christiansen syndrome.
Treatments for Bosma-Henkin-Christiansen syndrome: see treatments for Bosma-Henkin-Christiansen syndrome

Name and Aliases of Bosma-Henkin-Christiansen syndrome

Main name of condition: Bosma-Henkin-Christiansen syndrome

Other names or spellings for Bosma-Henkin-Christiansen syndrome:

hyposmia [nasal hypoplasia - hypogonadism], Hyposmia nasal hypoplasia hypogonadism

 

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