Cloacal exstrophy is a rare malformation that presents as a lower midline abdominal wall
defect which affects the gastrointestinal and genitourinary systems. The components of …

Omphalocele, exstrophy of cloaca, imperforate anus and spinal defect (OEIS Complex) is an
extremely rare combination of serious defects, which was firstly described by Carey and …

Cloacal exstrophy (CE) commonly referred to as the omphalocele, exstrophy of the bladder,
imperforate anus, and spinal abnormalities (OEIS) complex, is the least common …

Classically, cloacal exstrophy presents with omphalocele, bladder exstrophy, imperforate
anus, and spinal defects. We report a rare variant of cloacal exstrophy in a 6-day-old male …

Introduction The congenital anomaly of omphalocele, cloacal exstrophy, imperforate anus,
and spinal abnormalities (OEIS complex) is rare but well recognized. Hindgut duplications …

Cloacal exstrophy in its most complex form with OEIS syndrome is characterized by the
existence of an Omphalocele, Exstrophied bladder, Imperforate anus, and Spina bifida. We …

The omphalocele-exstrophy-imperforate anus-spinal defects (OEIS) complex is a rare birth
disorder involving a combination of gastrointestinal, musculoskeletal, renal, neural, and …

Exstrophy of the cloaca, a rare anomaly, is among the most complex malformations of
infancy. Features include omphalocele, imperforate anus, and exstrophy of two …

Cloacal exstrophy is a very rare and complicated birth defect. It occurs once in every
200,000 births. It is a complex anomaly of the urogenital tract and intestinal tract resulting in …

Cloacal exstrophy is the most severe type of anorectal malformations that belongs to the
bladder–exstrophy–epispadias complex of genitourinary malformations. Interestingly, its …