Seizures as the first manifestation of chromosome 22q11.2 deletion syndrome in a 40-year old man: a case report
<p>Abstract</p> <p>Background</p> <p>The microdeletion of chromosome 22q11.2 is the most common human deletion syndrome. It typically presents early in life and is rarely considered in adult patients. As part of the manifestations of this condition, patients can have pa...
Main Authors: | , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2007-12-01
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Series: | Journal of Medical Case Reports |
Online Access: | http://www.jmedicalcasereports.com/content/1/1/167 |