Symptoms vary and are very difficult to predict. Symptoms may not be as severe if you have both normal and abnormal cells.
Signs and tests
Genetic testing can diagnose mosaicism.
Tests will likely need to be repeated to confirm the results, and to help determine the type and severity of the disorder.
Treatment will depend on the type and severity of the disorder. You may need less intense treatment if only some of the cells are abnormal.
How well you do depend on which organs and tissues are affected (for example, the brain or heart). It is difficult to predict the effects of having two different cell lines in one person.
In general, patients with a high number of abnormal cells have the same outlook as people with the typical form of the disease (those who have all abnormal cells).
Patients with a low number of abnormal cells may only be mildly affected. They may not discover that they have mosaicism until they give birth to a child who has the typical (non-mosaic) form of the disease.
Complications depend on how many cells are affected by the genetic change.
Calling your health care provider
A diagnosis of mosaicism may cause confusion and uncertainty. A genetic counselor may help answer any questions about diagnosis and testing.
There is currently no known way to prevent mosaicism.
Chad Haldeman-Englert, MD, FACMG, Wake Forest School of Medicine, Department of Pediatrics, Section on Medical Genetics, Winston-Salem, NC. Review provided by VeriMed Healthcare Network. Also reviewed by A.D.A.M. Health Solutions, Ebix, Inc., Editorial Team: David Zieve, MD, MHA, David R. Eltz, and Stephanie Slon.