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Dictionary » R(12) syndrome
 

R(12) syndrome

Introduction: R(12) syndrome

Description of R(12) syndrome

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 as a Disease

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

Symptoms of R(12) syndrome (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)

Treatments for R(12) syndrome (Chromosome 12 ring syndrome) include:

  • Treatment varies considerable depending on the type and severity of symptom that develop
  • Surgery may be needed to correct defects or abnormalities e.g. heart defects, skull and facial abnormalities
  • Access to programs and services as required e.g. physical therapy, speech therapy, educational support, social, vocational and medical services
  • Various other symptomatic and supportive measures
  • Genetic counseling and joining a support group is recommended

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)

R(12) syndrome: Related Disease Topics

These medical disease topics may be related to R(12) syndrome:

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