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Chromosome 13 trisomy syndrome

Chromosome 13 trisomy syndrome: Introduction

Chromosome 13 trisomy syndrome: A rare chromosomal disorder where there are three copies of chromosome 13 rather than the normal two resulting in various abnormalities. Most die within months and there are few survivors after 10 years. More detailed information about the symptoms, causes, and treatments of Chromosome 13 trisomy syndrome is available below.

Symptoms of Chromosome 13 trisomy syndrome

Home Diagnostic Testing

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Chromosome 13 trisomy syndrome: Complications

Review possible medical complications related to Chromosome 13 trisomy syndrome:

  • Death during infancy or early childhood
  • Death #most die in early infancy
  • Death usually within 3 months #few survivors after 10 years
  • Death by ten years
  • more complications...»

Causes of Chromosome 13 trisomy syndrome

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Disease Topics Related To Chromosome 13 trisomy syndrome

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Less Common Symptoms of Chromosome 13 trisomy syndrome

Chromosome 13 trisomy syndrome: Research Doctors & Specialists

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Hospitals & Clinics: Chromosome 13 trisomy syndrome

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Statistics for Chromosome 13 trisomy syndrome

Chromosome 13 trisomy syndrome: Broader Related Topics

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Definitions of Chromosome 13 trisomy syndrome:

The presence of an additional (third) chromosome on an otherwise diploid chromosome 13 with variable abnormalities, most characteristic of which are microcephaly, microphthalmia, hypertelorism, cleft lip or palate, polydactyly, and cardiovascular, genitourinary, and neurological abnormalities. It is one of the most frequent causes of perinatal deaths. - (Source - Diseases Database)

Related Chromosome 13 trisomy syndrome Info

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More information about Chromosome 13 trisomy syndrome

  1. Chromosome 13 trisomy syndrome: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Home Testing
  6. Complications
 

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