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22q11.2 Deletion Syndrome - Patient Info
In 1965 DiGeorge described a patient with hypoparathyroidism and cellular immune deficiency secondary to thymic hypoplasia. Soon the pattern of malformation included in this syndrome expanded to include other defects of third and fourth branchial arches as well as dysmorphic facial features.
http://patient.info/doctor/22q112-deletion-syndrome
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What Is Chromosome 22q11.2 Deletion Syndrome, and Why Do You Need to Know? - Medscape
The chromosome 22q11.2 deletion is the most common microdeletion syndrome, which is actually quite perplexing because it's a condition that most clinicians have not heard about, partially due to the fact that it has had multiple names over the years.
http://www.medscape.com/viewarticle/866043
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22q11.2 Deletion Syndrome - NIH
22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2.
https://ghr.nlm.nih.gov/condition/22q112-deletion-syndrome
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22q11.2 Deletion Syndrome - Stanford Children
22q11.2 deletion syndrome is a genetic disorder. In this syndrome, a tiny piece of chromosome 22 is missing. This can cause many medical problems. These problems may range from heart defects and developmental delays to seizures and effects on facial appearance. These might include cleft palate (an opening in the roof of the mouth).
http://www.stanfordchildrens.org/en/topic/default?id=22q112-deletion-syndrome-90-P01682
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The 22q11 Deletion Syndromes
DiGeorge syndrome, velocardiofacial syndrome and various other malformations have been described in association with deletions and translocations involving human chromosome 22q11.
http://hmg.oxfordjournals.org/content/9/16/2421.full
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22q Fact Sheets
22q Deletion Syndrome (22q DS), which is also known as DiGeorge syndrome and Velo-Cardio-Facial syndrome, can affect many different parts of the body.
http://www.sickkids.ca/CGenetics/What-we-do/22q-deletion-syndrome-clinic/Meet-the-22q-team/index.html
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DiGeorge Syndrome - Mayo Clinic
DiGeorge syndrome (22q11.2 deletion syndrome) - Comprehensive overview covers causes, symptoms and treatment of this chromosomal disorder.
http://www.mayoclinic.org/diseases-conditions/digeorge-syndrome/basics/definition/con-20031464
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What is 22q11.2 Deletion Syndrome?
22q11.2 deletion syndrome is a genetic disorder. In this syndrome, a tiny piece of chromosome 22 is missing. This can cause many medical problems.
https://www.urmc.rochester.edu/Encyclopedia/Content.aspx?ContentTypeID=90
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Chromosome 22q11.2 Deletion Syndrome - NORD (National Organization for Rare Disorders)
Chromosome 22q11.2 deletion syndrome is associated with a range of problems including: congenital heart disease, palate abnormalities, immune system dysfunction including autoimmune disease, low calcium (hypocalcemia) and other endocrine abnormalities.
https://rarediseases.org/rare-diseases/chromosome-22q11-2-deletion-syndrome/
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DiGeorge Syndrome - Wikipedia, the Free Encyclopedia
22q11.2DS is the most common microdeletion syndrome characterized by low copy repeats and the deletion occurs near the middle of the chromosome at a location designated 22q11.2 - signifying its location on the long arm of one of the pair of chromosomes 22, on region 1, band 1, sub-band 2.
https://en.wikipedia.org/wiki/DiGeorge_syndrome
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About 22q11.2 Deletion Syndrome
22q11.2 Deletion Syndrome is a genetic disorder linked to a wide-range of health issues that is found in children where a small piece of chromosome 22 is missing.
http://www.nationwidechildrens.org/22q11-deletion-syndrome
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What is 22q? - Dempster Family Foundation
22q is a disorder caused by a small missing piece of the 22nd chromosome.
http://dempsterfamilyfoundation.org/what-22q/22q-overview
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Home - 22q.org
An easy way to share information about 22q with others!
http://www.22q.org
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22q11.2 Deletion Syndrome - Genetics Home Reference
22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece of chromosome 22.
http://ghr.nlm.nih.gov/condition/22q112-deletion-syndrome
