WITHDRAWN: Caudal duplication syndrome associated with caudal regression syndrome

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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...

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Caudal 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 ...

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Caudal Regression Syndrome

Caudal regression syndrome (CRS) is a rare neural tube defect affecting terminal spinal segments and cord manifesting as neurological deficit ranging from bladder and bowel involvement to severe sensory motor deficits in lower limbs. It has sporadic appearance and maternal diabetes, genetic factors, teratogens and hypoperfusion are considered as possible etiologic factors and it can be associat...

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Caudal regression syndrome.

INTRODUCTION The regression caudal syndrome includes a spectrum of malformations which vary from the symptomless coccygeal agenesis until thoracic vertebrae and sacrococcygeal agenesis with severe neurological deficit; it is associated sometimes with malformations in other organs and systems. We present a case of partial agenesis of sacro and coccix with neuromuscular, sphincter and orthopedist...

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Prenatal diagnosed caudal regression syndrome

Background: Caudal regression syndrome (CRS) is a rare complex congenital anomaly which is characterized by agenesis of the sacral and lumbar spine. Pelvis, lower extremity, genitourinary, cardiac anomalies and lower extremity neurological and motor development deficits may be accompanied. The exact etiology is unclear but the maternal insulin-dependent diabetes mellitus (hyperglycaemia during ...

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ژورنال

عنوان ژورنال: Journal of Pediatric Surgery Case Reports

سال: 2020

ISSN: 2213-5766

DOI: 10.1016/j.epsc.2020.101678