Dandy-Walker malformation

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Dandy-Walker Malformation

Dandy-Walker malformation is a rare congenital malformation and involves the cerebellum and fourth ventricle. The condition is characterized by agenesis or hypoplasia of the cerebellar vermis, cystic dilatation of the fourth ventricle, and enlargement of the posterior fossa. A large number of concomitant problems may be present, but the syndrome exists whenever these three features are found. A...

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Dandy-Walker Malformation Presenting with Psychological Manifestations

Dandy-Walker malformation, which is a congenital malformation of the cerebellum, is documented in literature to be associated with psychotic symptoms, obsessive compulsive symptoms, mood symptoms, hyperactivity, and impulsive behavior. The pathogenesis of psychiatric symptoms in Dandy-Walker malformation is thought to be due to disruption of the corticocerebellar tracts, resulting in what is kn...

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Dental Considerations in Dandy-Walker Malformation

Dandy-Walker malformation (DWM) is a congenital abnormality of the posterior cranial fossa with reported incidence of 1:25,000 to 1:35,000 live births [1,2]. The classic clinical trials of the DWM are absence of cerebellar vermis, cystic dilatation of the fourth ventricle, and the enlargement of posterior cranial fossa [3]. In approximately 80% of diagnosed DWM cases, the syndrome is accompanie...

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Dandy–Walker malformation: An incidental finding

Dandy-Walker malformation (DWM) is a rare intracranial congenital abnormality that affects the cerebellum and some of its components; particularly cerebellar vermis, fourth ventricle and is characterized by an enlarged posterior fossa. Although there is an extensive list of signs attributed to DWM, final diagnosis is solely dependent on imaging techniques as there are no signs that are characte...

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Dandy-Walker malformation: Surgical treatment of 17 cases

Seventeen patients with Dandy-Walker malformation were treated between 1985 and 2006. Hydrocephalus was present in 88% of patients at time of diagnosis. Cystoperitoneal and ventriculoperitoneal shunting were performed as primary modality of treatment in 2 and 13 cases respectively. Nine of them later required an additional shunting through a Y montage. Combined ventriculocystoperitoneal shuntin...

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ژورنال

عنوان ژورنال: Case Reports

سال: 2009

ISSN: 1757-790X

DOI: 10.1136/bcr.07.2008.0559