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Diseases » Tetrasomy X » Summary
 

What is Tetrasomy X?

What is Tetrasomy X?

  • Tetrasomy X: A rare chromosomal disorder which causes mental retardation, small head and various other anomalies.

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

Tetrasomy X: Introduction

Types of Tetrasomy X:

Broader types of Tetrasomy X:

How serious is Tetrasomy X?

Complications of Tetrasomy X: see complications of Tetrasomy X

What causes Tetrasomy X?

Causes of Tetrasomy X: see causes of Tetrasomy X

What are the symptoms of Tetrasomy X?

Symptoms of Tetrasomy X: see symptoms of Tetrasomy X

Complications of Tetrasomy X: see complications of Tetrasomy X

How is it treated?

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

Name and Aliases of Tetrasomy X

Main name of condition: Tetrasomy X

Other names or spellings for Tetrasomy X:

48 XXXX syndrome, 48 XXXX

48 XXXX, 48 XXXX syndrome
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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