DANDY WALKER MALFORMATION: A RARE CASE REPORT
- 1 September 2021
- journal article
- Published by World Wide Journals
Abstract
Dandy-Walker malformation (DWM) or syndrome is a posterior fossa anomaly characterized by agenesis or hypoplasia of the vermis and cystic enlargement of the fourth ventricle causing upward displacement of tentorium and torcula. Most patients have hydrocephalus at the time of diagnosis. DMW is the most common posterior fossa malformation, and it typically occurs sporadically. This is a case report of male fetus that was diagnosed to have Dandy Walker Malformation during the antenatal obstetric scans.Keywords
This publication has 7 references indexed in Scilit:
- Handbook of NeurosurgeryPublished by Georg Thieme Verlag KG ,2020
- Neuroimaging of Dandy-Walker MalformationTopics in Magnetic Resonance Imaging, 2011
- Linkage to chromosome 2q36.1 in autosomal dominant Dandy-Walker malformation with occipital cephalocele and evidence for genetic heterogeneityHuman Genetics, 2008
- Treatment options for Dandy–Walker malformationJournal of Neurosurgery: Pediatrics, 2006
- Closure of the cerebellar vermis: evaluation with second trimester US.Radiology, 1994
- Developmental NeuropathologyPublished by Springer Science and Business Media LLC ,1989
- The Dandy-Walker malformationJournal of Neurosurgery, 1984