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Diseases » Trisomy 6 » Summary
 

What is Trisomy 6?

What is Trisomy 6?

  • Trisomy 6: A rare chromosomal disorder involving the duplication of chromosome 6 which results in variable symptoms including mental retardation, retarded growth, facial anomalies and various other abnormalities. Full Trisomy 6 is results in spontaneous abortion whereas various degrees of Trisomy 6q can result in syndromes of variable severity depending on the size of the duplication.

Trisomy 6: Introduction

Types of Trisomy 6:

Broader types of Trisomy 6:

What causes Trisomy 6?

Causes of Trisomy 6: see causes of Trisomy 6

What are the symptoms of Trisomy 6?

Symptoms of Trisomy 6: see symptoms of Trisomy 6

Trisomy 6: Testing

Diagnostic testing: see tests for Trisomy 6.

How is it treated?

Doctors and Medical Specialists for Trisomy 6: Medical Geneticist ; see also doctors and medical specialists for Trisomy 6.
Treatments for Trisomy 6: see treatments for Trisomy 6
Research for Trisomy 6: see research for Trisomy 6

Name of Trisomy 6

Main name of condition: Trisomy 6

 

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