R(20) syndrome (medical condition): A rare chromosomal disorder where genetic material from one or both ends of chromosome 20 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 20 ring:
»Introduction: Chromosome 20 ring
»Symptoms of Chromosome 20 ring
R(20) syndrome: Another name for Chromosome 20 ring (or close medical condition association).
»Introduction: Chromosome 20 ring
»Symptoms of Chromosome 20 ring
Some of the symptoms of R(20) syndrome incude:
See full list of 20 symptoms of R(20) syndrome (Chromosome 20 ring)
These medical disease topics may be related to R(20) syndrome:
Search to find out more about R(20) syndrome:
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