| Literature DB >> 15662698 |
A Agangi1, D Paladini, P Bagolan, G M Maruotti, P Martinelli.
Abstract
Spilt notochord syndrome is an extremely rare form of spinal dysraphism characterized by a complete cleft of the spine and a persistent communication between endoderm and ectoderm. A variant of split notochord syndrome was diagnosed in a 25-week-old fetus showing a prolapsed congenital colostomy and a spinal cystic lesion. The final diagnosis included protruding colon segment, imperforate anus with a rectourethral fistula and lipomyelomeningocele. The ultrasound features of the condition and the post-natal management are discussed. The neonate was successfully treated with a posterior sagittal anorectoplasty, while the lipomyelomeningocele was resected at a later stage. Copyright (c) 2005 John Wiley & Sons, Ltd.Entities:
Mesh:
Year: 2005 PMID: 15662698 DOI: 10.1002/pd.1076
Source DB: PubMed Journal: Prenat Diagn ISSN: 0197-3851 Impact factor: 3.050