R(13) syndrome (medical condition): A rare chromosomal disorder where genetic material from one or both ends of chromosome 13 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 13 ring syndrome:
»Introduction: Chromosome 13 ring syndrome
»Symptoms of Chromosome 13 ring syndrome
»Treatments for Chromosome 13 ring syndrome
These medical condition or symptom topics may be relevant to medical information for R(13) syndrome:
R(13) syndrome: Another name for Chromosome 13 ring syndrome (or close medical condition association).
»Introduction: Chromosome 13 ring syndrome
»Symptoms of Chromosome 13 ring syndrome
»Treatments for Chromosome 13 ring syndrome
Some of the symptoms of R(13) syndrome incude:
See full list of 80 symptoms of R(13) syndrome (Chromosome 13 ring syndrome)
Treatments for R(13) syndrome (Chromosome 13 ring syndrome) include:
Read more about treatments for R(13) syndrome
Treatment of R(13) syndrome: For more treatment information about R(13) syndrome, see treatment of Chromosome 13 ring syndrome (R(13) syndrome)
These medical disease topics may be related to R(13) syndrome:
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