R(17) syndrome (medical condition): A rare chromosomal disorder where genetic material from one or both ends of chromosome 17 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 17 ring:
»Introduction: Chromosome 17 ring
»Symptoms of Chromosome 17 ring
R(17) syndrome: Another name for Chromosome 17 ring (or close medical condition association).
»Introduction: Chromosome 17 ring
»Symptoms of Chromosome 17 ring
Some of the symptoms of R(17) syndrome incude:
See full list of 23 symptoms of R(17) syndrome (Chromosome 17 ring)
These medical disease topics may be related to R(17) syndrome:
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