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4p16.3 deletion: A rare genetic disorder where a portion of chromosome 4 is deleted at a location called 16.3. The condition is characterized by malformations in most parts of the body as the deletion affects growth and development of the fetus. More detailed information about the symptoms, causes, and treatments of 4p16.3 deletion is available below.
See full list of 38 symptoms of 4p16.3 deletion
Review possible medical complications related to 4p16.3 deletion:
Book excerpts: Copyright © 2008 Lippincott Williams & Wilkins. All rights reserved.
See full list of 23 occasional symptoms of 4p16.3 deletion
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