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Chromosome 8, Monosomy 8p2: 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 8p2 is available below.
See full list of 38 symptoms of Chromosome 8, Monosomy 8p2
Read more about treatments for Chromosome 8, Monosomy 8p2
Read more about causes of Chromosome 8, Monosomy 8p2.
Prognosis for Chromosome 8, Monosomy 8p2: 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 8p2
Types of Chromosome 8, Monosomy 8p2
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Chromosome 8, Monosomy 8p2 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 8p2, or a subtype of Chromosome 8, Monosomy 8p2,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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