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7p2 Monosomy Syndrome: A rare chromosomal disorder where there is one copy of the end of the short arm (p) of chromosome 7 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 7p2 Monosomy Syndrome is available below.
Read more about causes of 7p2 Monosomy Syndrome.
Prognosis for 7p2 Monosomy Syndrome: 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.
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7p2 Monosomy Syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that 7p2 Monosomy Syndrome, or a subtype of 7p2 Monosomy Syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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