Assessment
Questionnaire

Have a symptom?
See what questions
a doctor would ask.
 

Chromosome 21, uniparental disomy of

Chromosome 21, uniparental disomy of: Introduction

Chromosome 21, uniparental disomy of: 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 21, uniparental disomy of is available below.

Symptoms of Chromosome 21, uniparental disomy of

Home Diagnostic Testing

Home medical testing related to Chromosome 21, uniparental disomy of:

Wrongly Diagnosed with Chromosome 21, uniparental disomy of?

Causes of Chromosome 21, uniparental disomy of

Read more about causes of Chromosome 21, uniparental disomy of.

Chromosome 21, uniparental disomy of: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Chromosome 21, uniparental disomy of

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, it can be over-diagnosed (it can, of course, also fail to be...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 measure blood pressure can simply...read more »

Children with migraine often misdiagnosed: A migraine often fails to be correctly diagnosed in pediatric patients. These patients are not the...read more »

Chromosome 21, uniparental disomy of: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Hospitals & Clinics: Chromosome 21, uniparental disomy of

Research quality ratings and patient safety measures for medical facilities in specialties related to Chromosome 21, uniparental disomy of:

Choosing the Best Hospital: More general information, not necessarily in relation to Chromosome 21, uniparental disomy of, on hospital performance and surgical care quality:

Statistics for Chromosome 21, uniparental disomy of

Chromosome 21, uniparental disomy of: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Chromosome 21, uniparental disomy of, or answer someone else's question, on our message boards:

Definitions of Chromosome 21, uniparental disomy of:

Chromosome 21, uniparental disomy of is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Chromosome 21, uniparental disomy of, or a subtype of Chromosome 21, uniparental disomy of, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related Chromosome 21, uniparental disomy of Info

Videos about Chromosome 21, uniparental disomy of

 

More information about Chromosome 21, uniparental disomy of

  1. Chromosome 21, uniparental disomy of: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.

Home | Symptoms | Diseases | Diagnosis | Videos | Tools | Forum | About Us | Terms of Use | Privacy Policy | Site Map | Advertise