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R(12) syndrome (medical condition): A rare chromosomal disorder where genetic material from one or both ends of chromosome 12 is missing and the two broken ends have rejoined to form a ring. The resulting type and severity of symptoms is determined by the amount and location of genetic material missing.
See also:
Chromosome 12 ring syndrome:
»Introduction: Chromosome 12 ring syndrome
»Symptoms of Chromosome 12 ring syndrome
»Treatments for Chromosome 12 ring syndrome
R(12) syndrome: Another name for Chromosome 12 ring syndrome (or close medical condition association).
»Introduction: Chromosome 12 ring syndrome
»Symptoms of Chromosome 12 ring syndrome
»Treatments for Chromosome 12 ring syndrome
Some of the symptoms of R(12) syndrome incude:
See full list of 19 symptoms of R(12) syndrome (Chromosome 12 ring syndrome)
Treatments for R(12) syndrome (Chromosome 12 ring syndrome) include:
Read more about treatments for R(12) syndrome
Treatment of R(12) syndrome: For more treatment information about R(12) syndrome, see treatment of Chromosome 12 ring syndrome (R(12) syndrome)
These medical disease topics may be related to R(12) syndrome:
Search to find out more about R(12) syndrome:
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