American Journal of Medical Genetics Part A · 2016 · 28 citations · 43 references
MedicineCardiologyPediatricsHuman GeneticsPediatric CardiologyPediatric PathologyCongenital Disorder EpidemiologyCongenital DisordersCongenital Heart DiseaseCardiac Developmental DefectsCongenital Cardiac AnomaliesCongenital Diaphragm AbnormalitiesDiaphragmatic AbnormalitiesEtiology Of Congenital Anomalies
We report the important association of congenital diaphragmatic hernia (CDH) and 22q11.2 deletion syndrome (22q11.2DS). The prevalence of CDH in our cohort of patients with 22q11.2DS is 0.8% (10/1246), which is greater than in the general population (0.025%). This observation suggests that 22q11.2DS should be considered when a child or fetus presents with CDH, in particular when other clinical findings associated with the 22q11.2DS are present, such as congenital cardiac defects. Furthermore, this finding may lead to the identification of an additional locus for diaphragmatic hernia in the general population. © 2016 Wiley Periodicals, Inc.
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Role of TBX1 in human del22q11.2 syndrome
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