Cloacal Exstrophy

Living reference work entry

Abstract

Cloacal exstrophy is a rare congenital malformation resulting in exstrophy of the urinary, intestinal, and genital systems and is associated with anomalies of other organ systems. The term OEIS complex (omphalocele, exstrophy of the bladder, imperforate anus, and spinal defects) is used to describe the spectrum of malformations in cloacal exstrophy (Carey and Greenbaum 1978; Kaya et al. 2000). The incidence of cloacal exstrophy is estimated to be 1/200,000–1/400,000 live births (Carey et al. 1978; Hurwitz et al. 1987; Dick et al. 2001), although the true incidence may be as high as 1 in 10,000–50,000, taking into account the lack of diagnosis in stillborn infants (Keppler-Noreuil 2001).

Keywords

Cage Hydrocephalus Dick Lipoma Hydronephrosis 

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Copyright information

© Springer Science+Business Media New York 2016

Authors and Affiliations

  1. 1.Medical GeneticsShriners Hospitals for ChildrenShreveportUSA
  2. 2.Perinatal and Clinical Genetics, Department of PediatricsLSU Health Sciences CenterShreveportUSA

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