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Chromosome 18, Monosomy 18p: A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material that is missing. More detailed information about the symptoms, causes, and treatments of Chromosome 18, Monosomy 18p is available below.
See full list of 50 symptoms of Chromosome 18, Monosomy 18p
Read more about treatments for Chromosome 18, Monosomy 18p
Read more about causes of Chromosome 18, Monosomy 18p.
Research the causes of these diseases that are similar to, or related to, Chromosome 18, Monosomy 18p:
Prognosis for Chromosome 18, Monosomy 18p: 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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Types of Chromosome 18, Monosomy 18p
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Chromosome 18, Monosomy 18p is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Chromosome 18, Monosomy 18p, or a subtype of Chromosome 18, Monosomy 18p,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
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