DiGeorge anomaly in a patient with isoch
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Ralph J. DeBerardinis; Livija Medne; Nancy B. Spinner; Elaine H. Zackai
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Article
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2005
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John Wiley and Sons
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English
⚖ 150 KB
👁 2 views
## Abstract The DiGeorge anomaly (DGA) is an etiologically heterogeneous developmental field defect in which cardiovascular malformations, hypocalcemia, thymic hypoplasia, and characteristic dysmorphisms are major clinical features. The 22q11.2 deletion is the most common single etiology of DGA, al