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X chromosome, monosomy Xq28

X chromosome, monosomy Xq28: Introduction

X chromosome, monosomy Xq28: A condition that is characterised by the occurrence of only one X chromosome in the genotype of an individual. More detailed information about the symptoms, causes, and treatments of X chromosome, monosomy Xq28 is available below.

Symptoms of X chromosome, monosomy Xq28

Causes of X chromosome, monosomy Xq28

Read more about causes of X chromosome, monosomy Xq28.

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Definitions of X chromosome, monosomy Xq28:

X chromosome, monosomy Xq28 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that X chromosome, monosomy Xq28, or a subtype of X chromosome, monosomy Xq28, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about X chromosome, monosomy Xq28

  1. X chromosome, monosomy Xq28: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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