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Chromosome 7, Monosomy

Chromosome 7, Monosomy: Introduction

Chromosome 7, Monosomy: A rare chromosomal disorder where there is one copy of the genetic material in chromosome 7 rather than the normal two. The deletion of this chromosome if often associated with myelodysplastic syndromes and myeloid leukemia. The condition usually has a poor prognosis. Other defects may also be present in some cases. More detailed information about the symptoms, causes, and treatments of Chromosome 7, Monosomy is available below.

Symptoms of Chromosome 7, Monosomy

Wrongly Diagnosed with Chromosome 7, Monosomy?

Chromosome 7, Monosomy: Complications

Review possible medical complications related to Chromosome 7, Monosomy:

Causes of Chromosome 7, Monosomy

Read more about causes of Chromosome 7, Monosomy.

Prognosis for Chromosome 7, Monosomy

Prognosis for Chromosome 7, Monosomy: The prognosis is usually poor with the majority dying due to the blood cancer. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.

Statistics for Chromosome 7, Monosomy

Chromosome 7, Monosomy: Broader Related Topics

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Definitions of Chromosome 7, Monosomy:

Chromosome 7, Monosomy is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 7, Monosomy, or a subtype of Chromosome 7, Monosomy, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 7, Monosomy

  1. Chromosome 7, Monosomy: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
  6. Prognosis
 

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