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Chromosome 8, Monosomy 8p21-pter: A rare chromosomal disorder where there is one copy of part of the short arm (p) of chromosome 8 rather than the normal two. The type and severity of symptoms is determined by the location and size of the genetic material deleted. More detailed information about the symptoms, causes, and treatments of Chromosome 8, Monosomy 8p21-pter is available below.
See full list of 27 symptoms of Chromosome 8, Monosomy 8p21-pter
Read more about treatments for Chromosome 8, Monosomy 8p21-pter
Read more about causes of Chromosome 8, Monosomy 8p21-pter.
Prognosis for Chromosome 8, Monosomy 8p21-pter: The prognosis varies considerably 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 8, Monosomy 8p21-pter
Types of Chromosome 8, Monosomy 8p21-pter
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Chromosome 8, Monosomy 8p21-pter is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 8, Monosomy 8p21-pter, or a subtype of Chromosome 8, Monosomy 8p21-pter,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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