DiGeorge anomaly with renal agenesis in infants of mothers with diabetes
β Scribed by Wilson, Thomas A. ;Blethen, Sandra L. ;Vallone, Ambrose ;Alenick, D. Scott ;Nolan, Patricia ;Katz, Arnold ;Amorillo, Thomas P. ;Goldmuntz, Elizabeth ;Emanuel, Beverly S. ;Driscoll, Deborah A.
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 477 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0148-7299
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## 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
Despite advances in therapy for maternal diabetes, pregnancies of diabetic women remained at an increased risk of spontaneous abortion or delivery of an infant with major malformation. We report on an infant of a diabetic mother with hypoglossia-hypodactylia associated with complete jejunal atresia.