Features of Diagnosing and Managing a Patient with DiGeorge Syndrome
The article presents a case of own clinical observation of DiGeorge syndrome (22q11.2 chromosome deletion syndrome) in a child. The features of the disease course with the dominance of clinical symptoms of congenital malformations of the heart, blood vessels and lungs are noted. This case demonstrat...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
Zaslavsky O.Yu.,
2016-04-01T00:00:00Z.
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