منابع مشابه
Caudal duplication syndrome.
CASE A female infant, born by cesarean delivery (dilation dystocia), was referred to our service at age of 24 hours with a history of “imperforate anus”. Physical examination revealed duplicity of the vulvar introit (urine output by the right orifice and feces by the left). She was submitted to the following imaging exams: (1) echodopplercardiogram – interatrial and interventricular communicati...
متن کاملCaudal duplication syndrome.
Complete duplication of genitourinary system, colon and vertebral column is a very rare and complex congenital condition termed as "caudal duplication syndrome" with variable presentations. This term is often quoted as a type of incomplete separation of mono-ovular twins or conjoined twinning. It is associated with other congenital malformations of the genitourinary, gastrointestinal and other ...
متن کاملDuplication of Peno-Scroto-Testicular Unit- A Rare Form of Caudal Duplication Syndrome
Duplication of penis has been reported to occur once in every 5 to 6 million live births.[1] It presents as duplication of only glans to complete duplication of the phallus and usually associated with other anomalies like bifid scrotum, double bladder, vertebral anomalies and ano-rectal malformations etc.[2] With this backdrop, herein we present a newborn with complete duplication of the entire...
متن کاملCaudal Duplication Syndrome: the Vital Role of a Multidisciplinary Approach and Staged Correction
Caudal duplication syndrome is a rare entity that describes the association between congenital anomalies involving caudal structures and may have a wide spectrum of clinical manifestations. A full-term male presented with combination of anomalies including anorectal malformation, duplication of the colon and lower urinary tract, split of the lower spine, and lipomyelomeningocele with tethering ...
متن کاملCaudal duplication syndrome: imaging evaluation of a rare entity in an adult patient.
Several theories have been put forth to explain the complex yet symmetrical malformations and the myriad of clinical presentations of caudal duplication syndrome. Hereby, reported case is a 28-year-old female, gravida 2 para 2, with congenital caudal malformation who has undergone partial reconstructive surgeries in infancy to connect her 2 colons. She presented with recurrent left lower abdomi...
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ژورنال
عنوان ژورنال: Arquivos de Neuro-Psiquiatria
سال: 2009
ISSN: 0004-282X
DOI: 10.1590/s0004-282x2009000400023