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Chromosome 16, uniparental disomy

Chromosome 16, uniparental disomy: Introduction

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

Home Diagnostic Testing

Home medical testing related to Chromosome 16, uniparental disomy:

Wrongly Diagnosed with Chromosome 16, uniparental disomy?

Causes of Chromosome 16, uniparental disomy

Read more about causes of Chromosome 16, uniparental disomy.

Less Common Symptoms of Chromosome 16, uniparental disomy

Chromosome 16, uniparental disomy: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Chromosome 16, uniparental disomy

Mild worm infections undiagnosed in children: Human worm infestations, esp. threadworm, can be overlooked in some cases, because it may cause only mild or even absent symptoms. Although the most common symptoms are anal itch (or ...read more »

Mesenteric adenitis misdiagnosed as appendicitis in children: Because appendicitis is one of the more feared conditions for a child with abdominal pain,...read more »

Blood pressure cuffs misdiagnose hypertension in children: One known misdiagnosis issue with hyperension, arises in relation to the simple equipment used to test blood pressure. The "cuff" around the arm to...read more »

Children with migraine often misdiagnosed: A migraine often fails to be correctly diagnosed in pediatric patients. These patients are not the typical migraine sufferers, but migraines can also occur in children. See ...read more »

Chromosome 16, uniparental disomy: Research Doctors & Specialists

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Hospitals & Clinics: Chromosome 16, uniparental disomy

Research quality ratings and patient safety measures for medical facilities in specialties related to Chromosome 16, uniparental disomy:

Choosing the Best Hospital: More general information, not necessarily in relation to Chromosome 16, uniparental disomy, on hospital performance and surgical care quality:

Statistics for Chromosome 16, uniparental disomy

Chromosome 16, uniparental disomy: Broader Related Topics

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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)

Related Chromosome 16, uniparental disomy Info

Videos about Chromosome 16, uniparental disomy

 

More information about Chromosome 16, uniparental disomy

  1. Chromosome 16, uniparental disomy: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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