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Chromosome 1, trisomy 1q32 qter

Chromosome 1, trisomy 1q32 qter: Introduction

Chromosome 1, trisomy 1q32 qter: A rare chromosomal disorder where duplication of a portion of chromosome 1 causes various abnormalities such as retarded fetal growth, facial anomalies, mental retardation, stillbirth, heart defects and finger and toe abnormalities. More detailed information about the symptoms, causes, and treatments of Chromosome 1, trisomy 1q32 qter is available below.

Symptoms of Chromosome 1, trisomy 1q32 qter

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Causes of Chromosome 1, trisomy 1q32 qter

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Disease Topics Related To Chromosome 1, trisomy 1q32 qter

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Definitions of Chromosome 1, trisomy 1q32 qter:

Chromosome 1, trisomy 1q32 qter is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 1, trisomy 1q32 qter, or a subtype of Chromosome 1, trisomy 1q32 qter, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Chromosome 1, trisomy 1q32 qter

  1. Chromosome 1, trisomy 1q32 qter: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
 

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