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Monosomy 13q14

Monosomy 13q14: Introduction

Monosomy 13q14: Deletions of genetic material from a specific area of chromosome 13 (q14) has been strongly linked to the development of myeloid malignancies such as chronic lymphocytic leukemia, acute myeloid leukemia, myeloproliferative disorders and myelodysplastic syndromes. More detailed information about the symptoms, causes, and treatments of Monosomy 13q14 is available below.

Symptoms of Monosomy 13q14

  • Increased risk of developing myeloproliferative disorders
  • Increased risk of developing myelodysplastic syndromes
  • Increased risk of developing acute myeloid leukemia
  • Increased risk of developing chronic lymphocytic leukemia
  • Increased risk of developing myeloid malignancies
  • more symptoms...»

Causes of Monosomy 13q14

Read more about causes of Monosomy 13q14.

Statistics for Monosomy 13q14

Monosomy 13q14: Broader Related Topics

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Definitions of Monosomy 13q14:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Monosomy 13q14 as a "rare disease".
Source - Orphanet

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More information about Monosomy 13q14

  1. Monosomy 13q14: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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