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Chromosome 16, uniparental disomy
Introduction: Chromosome 16, uniparental disomy
Chromosome 16, uniparental disomy: A rare chromosomal disorder where an extra copy of chromosome 16 is inherited from one parent only. More detailed information about the symptoms, causes, and treatments of Chromosome 16, uniparental disomy is available below.
Symptoms of Chromosome 16, uniparental disomy
- Retarded fetal growth
- Stillbirth
- Low birth weight
- Premature membrane rupture during pregnancy
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Less Common Symptoms of Chromosome 16, uniparental disomy
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Wrongly Diagnosed with Chromosome 16, uniparental disomy?
Misdiagnosis and Chromosome 16, uniparental disomy
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Definitions of Chromosome 16, uniparental disomy:
Chromosome 16, uniparental disomy is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 16, uniparental disomy, or a subtype of Chromosome 16, uniparental disomy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
- Chromosome 16, uniparental disomy
- What is Chromosome 16, uniparental disomy?
- Prevalence and Incidence of Chromosome 16, uniparental disomy
- Videos related to Chromosome 16, uniparental disomy
- Symptoms of Chromosome 16, uniparental disomy
- Diagnostic Tests for Chromosome 16, uniparental disomy
- Signs of Chromosome 16, uniparental disomy
- Misdiagnosis of Chromosome 16, uniparental disomy
- Treatments for Chromosome 16, uniparental disomy
- Glossary for Chromosome 16, uniparental disomy
» Next page: What is Chromosome 16, uniparental disomy?
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- What is Chromosome 16, uniparental disomy?
- Prevalence and Incidence of Chromosome 16, uniparental disomy
- Videos related to Chromosome 16, uniparental disomy
- Symptoms of Chromosome 16, uniparental disomy
- Diagnostic Tests for Chromosome 16, uniparental disomy
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