| Literature DB >> 10998453 |
G V Velagaleti1, A Kumar, L H Lockhart, R Matalon.
Abstract
We describe an uncommon association of deletion 22q11 in a patient with Klinefelter syndrome. Even though congenital heart defects (CHD) are not associated with Klinefelter syndrome, further investigation of this patient with patent ductus arteriosus showed a microdeletion of chromosome 22q11.2. While this finding may be coincidental, it is important to further evaluate patients when the clinical features are suggestive of a secondary abnormality.Entities:
Mesh:
Year: 2000 PMID: 10998453 DOI: 10.1016/s0003-3995(00)01013-3
Source DB: PubMed Journal: Ann Genet ISSN: 0003-3995