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What is Buntinx-Lormans-Martin syndrome?

What is Buntinx-Lormans-Martin syndrome?

  • Buntinx-Lormans-Martin syndrome: A very rare syndrome characterized mainly by eye anomalies and fusion of the forearm bones.

Buntinx-Lormans-Martin syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Buntinx-Lormans-Martin syndrome, or a subtype of Buntinx-Lormans-Martin syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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

Buntinx-Lormans-Martin syndrome: Introduction

Types of Buntinx-Lormans-Martin syndrome:

Broader types of Buntinx-Lormans-Martin syndrome:

What causes Buntinx-Lormans-Martin syndrome?

Causes of Buntinx-Lormans-Martin syndrome: see causes of Buntinx-Lormans-Martin syndrome

What are the symptoms of Buntinx-Lormans-Martin syndrome?

Symptoms of Buntinx-Lormans-Martin syndrome: see symptoms of Buntinx-Lormans-Martin syndrome

Buntinx-Lormans-Martin syndrome: Testing

Diagnostic testing: see tests for Buntinx-Lormans-Martin syndrome.

Misdiagnosis: see misdiagnosis and Buntinx-Lormans-Martin syndrome.

How is it treated?

Doctors and Medical Specialists for Buntinx-Lormans-Martin syndrome: Pediatrician, Orthopedic Surgeon ; see also doctors and medical specialists for Buntinx-Lormans-Martin syndrome.
Treatments for Buntinx-Lormans-Martin syndrome: see treatments for Buntinx-Lormans-Martin syndrome

Name and Aliases of Buntinx-Lormans-Martin syndrome

Main name of condition: Buntinx-Lormans-Martin syndrome

Other names or spellings for Buntinx-Lormans-Martin syndrome:

Radioulnar synostosis retinal pigment abnormalities, Radioulnar synostosis [retinal pigment abnormalities]


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