Uniparental disomy: Introduction
Uniparental disomy: A condition which is characterised by the uniparental disomy of chromosomes.
More detailed information about the symptoms,
causes, and treatments of Uniparental disomy is available below.
Symptoms of Uniparental disomy
See full list of 11
symptoms of Uniparental disomy
Home Diagnostic Testing
Home medical testing related to Uniparental disomy:
Wrongly Diagnosed with Uniparental disomy?
Causes of Uniparental disomy
Read more about causes of Uniparental disomy.
Uniparental disomy: Undiagnosed Conditions
Commonly undiagnosed diseases in related medical categories:
Misdiagnosis and 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...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 diagnosed with fatal...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...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 »
Read more about Misdiagnosis and Uniparental disomy
Uniparental disomy: Research Doctors & Specialists
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Hospitals & Clinics: Uniparental disomy
Research quality ratings and patient safety measures
for medical facilities in specialties related to Uniparental disomy:
Hospital & Clinic quality ratings »
Choosing the Best Hospital:
More general information, not necessarily in relation to Uniparental disomy,
on hospital performance and surgical care quality:
Evidence Based Medicine Research for Uniparental disomy
Medical research articles related to Uniparental disomy include:
Click here to find more evidence-based articles on the TRIP Database
Research about Uniparental disomy
Visit our research pages for current research about Uniparental disomy treatments.
Statistics for Uniparental disomy
Uniparental disomy: Broader Related Topics
Types of Uniparental disomy
User Interactive Forums
Read about other experiences, ask a question about Uniparental disomy, or answer someone else's question, on our message boards:
Definitions of Uniparental disomy:
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 Uniparental disomy, or a subtype of Uniparental disomy,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Uniparental disomy as a "rare disease".
Source - Orphanet
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