Jacobsen Syndrome Rare Disorders Conditions and Diseases

Jacobsen Syndrome

Jacobsen Syndrome (11q Deletion, or 11q-) is a rare chromosomal abnormality which affects perhaps one child in 100,000 in which a portion of the 11th chromosome is missing. It was discovered by Dr. P. Jacobsen in 1973. At that time, the disease was named "Jacobsen Syndrome."

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• - Clinical synopsis, plus research summaries.
  
• - Includes a reference database, family support groups and clinical information.
  
  

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