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R(6) syndrome (medical condition): A rare chromosomal disorder where the ends of chromosome 6 have been deleted and the two broken ends have rejoined to form a ring shape resulting in a range of symptoms determined by the size of the genetic deletion.
See also:
Chromosome 6 ring syndrome:
»Introduction: Chromosome 6 ring syndrome
»Symptoms of Chromosome 6 ring syndrome
»Treatments for Chromosome 6 ring syndrome
R(6) syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that R(6) syndrome, or a subtype of R(6) syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
R(6) syndrome: Another name for Chromosome 6 ring syndrome (or close medical condition association).
»Introduction: Chromosome 6 ring syndrome
»Symptoms of Chromosome 6 ring syndrome
»Treatments for Chromosome 6 ring syndrome
Some of the symptoms of R(6) syndrome incude:
See full list of 31 symptoms of R(6) syndrome (Chromosome 6 ring syndrome)
Treatments for R(6) syndrome (Chromosome 6 ring syndrome) include:
Read more about treatments for R(6) syndrome
Treatment of R(6) syndrome: For more treatment information about R(6) syndrome, see treatment of Chromosome 6 ring syndrome (R(6) syndrome)
These medical disease topics may be related to R(6) syndrome:
Source - NIH
Search to find out more about R(6) syndrome:
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