Chromosome 1, uniparental disomy 1q12 q21: A rare chromosomal disorder where part or all of the short arm (p) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion. More detailed information about the symptoms, causes, and treatments of Chromosome 1, uniparental disomy 1q12 q21 is available below.
See full list of 75 symptoms of Chromosome 1, uniparental disomy 1q12 q21
Read more about treatments for Chromosome 1, uniparental disomy 1q12 q21
Home medical testing related to Chromosome 1, uniparental disomy 1q12 q21:
Read more about causes of Chromosome 1, uniparental disomy 1q12 q21.
Commonly undiagnosed diseases in related medical categories:
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...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...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 »
Read more about Misdiagnosis and Chromosome 1, uniparental disomy 1q12 q21
Research related physicians and medical specialists:
Other doctor, physician and specialist research services:
Research quality ratings and patient safety measures for medical facilities in specialties related to Chromosome 1, uniparental disomy 1q12 q21:
Hospital & Clinic quality ratings »
Choosing the Best Hospital: More general information, not necessarily in relation to Chromosome 1, uniparental disomy 1q12 q21, on hospital performance and surgical care quality:
Prognosis for Chromosome 1, uniparental disomy 1q12 q21: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.
More about prognosis of Chromosome 1, uniparental disomy 1q12 q21
Types of Chromosome 1, uniparental disomy 1q12 q21
Read about other experiences, ask a question about Chromosome 1, uniparental disomy 1q12 q21, or answer someone else's question, on our message boards:
Chromosome 1, uniparental disomy 1q12 q21 is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 1, uniparental disomy 1q12 q21, or a subtype of Chromosome 1, uniparental disomy 1q12 q21,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Tools & Services:
Medical Articles:
Search Specialists by State and City
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.
Copyright © 2011 Health Grades Inc. All rights reserved. Last Update: 7 May, 2013 (4:34)
