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Dictionary » R22
 

R22

Introduction: R22

Description of R22

R22 (medical condition): A rare chromosomal disorder where genetic material from one or both ends of chromosome 22 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 22 Ring:
  »Introduction: Chromosome 22 Ring
  »Symptoms of Chromosome 22 Ring
  »Treatments for Chromosome 22 Ring

R22: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

R22 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that R22, or a subtype of R22, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

R22 as a Disease

R22: Another name for Chromosome 22 Ring (or close medical condition association).
  »Introduction: Chromosome 22 Ring
  »Symptoms of Chromosome 22 Ring
  »Treatments for Chromosome 22 Ring

Symptoms of R22 (Chromosome 22 Ring)

Some of the symptoms of R22 incude:

See full list of 55 symptoms of R22 (Chromosome 22 Ring)

Treatments for R22 (Chromosome 22 Ring)

Treatments for R22 (Chromosome 22 Ring) 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 R22

Treatment of R22: For more treatment information about R22, see treatment of Chromosome 22 Ring (R22)

Terms associated with R22:

Terms Similar to R22:

Source - NIH

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