R(18) syndrome (medical condition): A rare chromosomal disorder where genetic material from one or both ends of chromosome 18 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 18 Ring:
»Introduction: Chromosome 18 Ring
»Symptoms of Chromosome 18 Ring
These medical condition or symptom topics may be relevant to medical information for R(18) syndrome:
R(18) syndrome: Another name for Chromosome 18 Ring (or close medical condition association).
»Introduction: Chromosome 18 Ring
»Symptoms of Chromosome 18 Ring
Some of the symptoms of R(18) syndrome incude:
See full list of 22 symptoms of R(18) syndrome (Chromosome 18 Ring)
These medical disease topics may be related to R(18) syndrome:
Search to find out more about R(18) syndrome:
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