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Monosomy 20p: A rare chromosomal disorder where the short arm (p) of chromosome 20 is deleted resulting in various abnormalities. The type and severity of symptoms varies depending on the amount and exact location of the genetic material that is deleted. More detailed information about the symptoms, causes, and treatments of Monosomy 20p is available below.
Read more about causes of Monosomy 20p.
Prognosis for Monosomy 20p: 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.
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Monosomy 20p is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Monosomy 20p, or a subtype of Monosomy 20p,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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