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8p-Syndrome, partial is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that 8p-Syndrome, partial, or a subtype of 8p-Syndrome, partial,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
8p-Syndrome, partial: Introduction
Broader types of 8p-Syndrome, partial:
Prognosis of 8p-Syndrome, partial: 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.
Causes of 8p-Syndrome, partial: see causes of 8p-Syndrome, partial
Symptoms of 8p-Syndrome, partial: see symptoms of 8p-Syndrome, partial
Doctors and Medical Specialists for 8p-Syndrome, partial: Medical Geneticist
;
see also doctors and medical specialists for 8p-Syndrome, partial.
Treatments for 8p-Syndrome, partial:
see treatments for 8p-Syndrome, partial
Main name of condition: 8p-Syndrome, partial
Other names or spellings for 8p-Syndrome, partial:
Chromosome 8, monosomy 8p21-pter, Chromosome 8, partial deletion (short arm), Chromosome 8, partial monosomy 8p2, Chromosome 8, monosomy 8p2, 8p deletion syndrome (partial)
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
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