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Fetal Pediatr Pathol ; 35(2): 133-41, 2016.
Article in English | MEDLINE | ID: mdl-26881326

ABSTRACT

We report a term female neonate with vertebral anomalies, anal and urethral atresia, esophageal atresia with tracheoesophageal fistula (TEF), renal agenesis, pulmonary hypoplasia, genital and sacral appendages, and a single umbilical artery. Genetic studies revealed a 20.91 Mb interstitial deletion of the long arm of X chromosome: Xq25-q27.3. This is a new case of VATER/VACTERL association with Xq25 microdeletion.


Subject(s)
Anal Canal/abnormalities , Anus, Imperforate/genetics , Chromosomes, Human, X/genetics , Esophagus/abnormalities , Gene Deletion , Heart Defects, Congenital/genetics , Kidney/abnormalities , Limb Deformities, Congenital/genetics , Radius/abnormalities , Spine/abnormalities , Trachea/abnormalities , Female , Humans , Infant, Newborn
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