Chromosome 22q11.2 deletion syndrome: A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans. More detailed information about the symptoms, causes, and treatments of Chromosome 22q11.2 deletion syndrome is available below.
See full list of 19 symptoms of Chromosome 22q11.2 deletion syndrome
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Research the causes of these diseases that are similar to, or related to, Chromosome 22q11.2 deletion syndrome:
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Heart attacks can be undiagnosed: Although the most severe symptoms of heart attack are hard to miss, there are varying degrees of severity. It is altogether too common for people to die from undiagnosed heart...read more »
Heart attacks can be overdiagnosed: Although many people die from heart attacks, there are also many cases where people fear that they have a...read more »
Rare heart condition often undiagnosed: The rare heart condition called long QT syndrome can lead to episodes of palpitations and rapid heartbeat. In rare...read more »
Heart attack can be over-diagnosed: Although heart attack is often undiagnosed, leading to fatality, it can also be over-diagnosed. People become concerned that a...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...read more »
Hypertension misdiagnosis common in children: Hypertension is often misdiagnosed in adults (see misdiagnosis of hypertension), but its misdiagnosis is even more likely in...read more »
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