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What is Viljoen Kallis Voges syndrome?

What is Viljoen Kallis Voges syndrome?

Viljoen Kallis Voges syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Viljoen Kallis Voges syndrome, or a subtype of Viljoen Kallis Voges 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 Viljoen Kallis Voges syndrome as a "rare disease".
Source - Orphanet

Viljoen Kallis Voges syndrome: Introduction

What are the symptoms of Viljoen Kallis Voges syndrome?

Symptoms of Viljoen Kallis Voges syndrome: see symptoms of Viljoen Kallis Voges syndrome

How is it treated?

Doctors and Medical Specialists for Viljoen Kallis Voges syndrome: Pediatrician ; see also doctors and medical specialists for Viljoen Kallis Voges syndrome.
Treatments for Viljoen Kallis Voges syndrome: see treatments for Viljoen Kallis Voges syndrome

Name and Aliases of Viljoen Kallis Voges syndrome

Main name of condition: Viljoen Kallis Voges syndrome

Other names or spellings for Viljoen Kallis Voges syndrome:

Microcephaly [brachydactyly - kyphoscoliosis], Microcephaly, short stature, brachydactyly type D, flattened occiput, low-set large ears, prominent nose, kyphoscoliosis and mental retardation

Microcephaly, short stature, brachydactyly type D, flattened occiput, low-set large ears, prominent nose, kyphoscoliosis and mental retardation
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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