Lagay, Kelleher, & Langer, …show more content…
Omphalocele can also be a symptom of this hereditary syndrome (Chen, 2007). Miller-Dieker lissencephaly syndrome, or MDLS, results from a deletion on chromosome
17p13.3 and is inherited in an autosomal dominant manner. Characteristic features include microcephaly and a small brain lacking gyri or convolutions. Omphalocele has been reported as prenatal identifier of this condition (Chen, 2007). Omphalocele has also been described as part of certain malformation sequences, including ectopia cordis, body stalk anomaly, and OEIS (Omphalocele, Exstrophy of bladder,
Imperforate anus, Spinal defect), as well as non-syndromic multiple congenital anomalies (Stoll,
Alembik, Dott, & Roth, 2008). Outside of genetic causes, additional factors correlated with an increased risk for omphalocele include smoking and using alcohol (Mac Bird, Robbins,
Druschel, Cleves, Yang, & Hobbs, 2009), using certain medications such as selective seratonin reuptake inhibitors (SSRIs) during pregnancy (Alwan, Reefhuis, Rasmussen, Olney, &
Friedman, 2007), and being overweight or obese prior to pregnancy (Waller, Shaw, Rasmussen,
Hobbs, Canfield, Siega-Riz,…& Correa,