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Diseases » Rathburn disease » Summary
 

What is Rathburn disease?

What is Rathburn disease?

  • Rathburn disease: A rare inherited condition involving bone and teeth mineralization abnormalities and reduced phosphatase enzyme activity. The severity of the disorder varies according to the degree of reduction in phosphatase activity.

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

Rathburn disease: Introduction

Types of Rathburn disease:

Broader types of Rathburn disease:

How serious is Rathburn disease?

Complications of Rathburn disease: see complications of Rathburn disease

What causes Rathburn disease?

Causes of Rathburn disease: see causes of Rathburn disease

What are the symptoms of Rathburn disease?

Symptoms of Rathburn disease: see symptoms of Rathburn disease

Complications of Rathburn disease: see complications of Rathburn disease

How is it treated?

Doctors and Medical Specialists for Rathburn disease: Medical Geneticist ; see also doctors and medical specialists for Rathburn disease.
Treatments for Rathburn disease: see treatments for Rathburn disease

Name and Aliases of Rathburn disease

Main name of condition: Rathburn disease

Other names or spellings for Rathburn disease:

Hypophosphatasia, Phosphoethanolaminuria

 

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