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Chromosome 11q Partial Deletion
Jacobsen syndrome
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Overview
Chromosome 11q partial deletion, also known as Jacobsen syndrome, is a rare genetic condition. This condition results from a mutation or error in a person’s DNA or genes. This can cause birth defects affecting the head, face, eyes, and hands, as well as abnormally slow growth and moderate to severe delays in skill learning. Although there is currently no cure for Jacobsen syndrome, there are various resources to help manage the condition and treat birth defects. Doctors seek help from various therapists and community services to provide support and care for families affected by Jacobsen syndrome.
Trusted Medical Sites
Genetic & Rare Diseases Information Center (GARD)
GARD provides the public with access to current, reliable, and easy-to-understand information about rare or genetic diseases in English or Spanish.
Support Organizations
Support organizations can provide help and guidance in areas such as peer matching, education and training, and therapy and counseling.