Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

The course of Dandy — Walker syndrome in a child withEdwards syndrome

View through CrossRef
Background. Dandy – Walker syndrome (Dandy – Walker syndrome) is a combined malformation of the brain, the identification of which may be an indication for expanding the diagnostic search in order to detect other malformations or chromosomal pathologies. It is characterized by dysgenesis of the cerebellar vermis, cystic enlargement of the fourth ventricle and an enlarged posterior cranial fossa, as a result of which the sinuses of the meninges and the cerebellum are shifted. The frequency of occurrence ranges from 1:5000 to 1:25000. Agenesia or hypoplasia of the cerebellar vermis in combination with other malformations of the brain are diagnosed already with screening ultrasound scanning of the fetus, however, the diagnosis of Dandy – Walker syndrome is made only after birth based on the manifestations of this syndrome during neuroimaging and genetic studies. In addition to the above changes in the cerebellum, Dandy – Walker syndrome is associated with hydrocephalus, agenesis of the corpus callosum, and other malformations of the central nervous system. The mechanism of development of hydrocephalus in Dandy – Walker syndrome is due to the blockage of normal spinal blood flow, resulting in defects in the holes of Magendie and Luschka. It is characterized by a wide clinical polymorphism. Basically, the first clinical symptoms are diagnosed already in the neonatal period. Objective. The article presents the course of Dandy – Walker syndrome in a child with trisomy 18 (Edwards syndrome). Conclusion. The unfavorable course of this syndrome is most often associated with the presence of concomitant pathology. The severity of clinical manifestations depends on the variant of the syndrome and the rate of progression of disorders. It is often diagnosed in children with chromosomal abnormalities, which complicates the period of early neonatal adaptation, requires the organization of special care and surgical correction of existing malformations. The presence of an infectious process in children with Dandy – Walker syndrome and chromosomal abnormalities can lead to multiple organ failure and deterioration of the child's condition.
Title: The course of Dandy — Walker syndrome in a child withEdwards syndrome
Description:
Background.
Dandy – Walker syndrome (Dandy – Walker syndrome) is a combined malformation of the brain, the identification of which may be an indication for expanding the diagnostic search in order to detect other malformations or chromosomal pathologies.
It is characterized by dysgenesis of the cerebellar vermis, cystic enlargement of the fourth ventricle and an enlarged posterior cranial fossa, as a result of which the sinuses of the meninges and the cerebellum are shifted.
The frequency of occurrence ranges from 1:5000 to 1:25000.
Agenesia or hypoplasia of the cerebellar vermis in combination with other malformations of the brain are diagnosed already with screening ultrasound scanning of the fetus, however, the diagnosis of Dandy – Walker syndrome is made only after birth based on the manifestations of this syndrome during neuroimaging and genetic studies.
In addition to the above changes in the cerebellum, Dandy – Walker syndrome is associated with hydrocephalus, agenesis of the corpus callosum, and other malformations of the central nervous system.
The mechanism of development of hydrocephalus in Dandy – Walker syndrome is due to the blockage of normal spinal blood flow, resulting in defects in the holes of Magendie and Luschka.
It is characterized by a wide clinical polymorphism.
Basically, the first clinical symptoms are diagnosed already in the neonatal period.
Objective.
The article presents the course of Dandy – Walker syndrome in a child with trisomy 18 (Edwards syndrome).
Conclusion.
The unfavorable course of this syndrome is most often associated with the presence of concomitant pathology.
The severity of clinical manifestations depends on the variant of the syndrome and the rate of progression of disorders.
It is often diagnosed in children with chromosomal abnormalities, which complicates the period of early neonatal adaptation, requires the organization of special care and surgical correction of existing malformations.
The presence of an infectious process in children with Dandy – Walker syndrome and chromosomal abnormalities can lead to multiple organ failure and deterioration of the child's condition.

Related Results

Manajemen Neuroanestesi pada Sindrom Dandy Walker dengan Hiperkalemia
Manajemen Neuroanestesi pada Sindrom Dandy Walker dengan Hiperkalemia
Sindrom Dandy Walker termasuk hidrosefalus yang sangat jarang terjadi dengan insiden 1 kasus dari 65 kasus hidrosefalus berdasarkan penelitian profil hidrosefalus di RSUDZA Banda A...
The Dandy
The Dandy
The dandy is a central figure in 19th-century constructions of masculinity and social class, associated principally with men who devote fastidious attention to dress. That broad em...
Manifestasi Klinis dan Neuroimaging Pada Sindrom Dandy Walker
Manifestasi Klinis dan Neuroimaging Pada Sindrom Dandy Walker
Dandy Walker syndrome is a rare malforation of the central nervous system characterized by expansion of the fourth ventricle, widening of the posterior fossa, agenesis or dysplasia...
Cystoperitoneal Shunting for Patient with Hydrocephalus Associated with Aqueductal Obstruction in Dandy-Walker Malformation: A Case Report
Cystoperitoneal Shunting for Patient with Hydrocephalus Associated with Aqueductal Obstruction in Dandy-Walker Malformation: A Case Report
Dandy-Walker Malformation presents as a congenital anomaly that affects the posterior fossa. Presenting hydrocephalus as secondary to Dandy-Walker Malformation is the main concern...
The Beardsleyan Dandy: Icon of Grotesque Beauty
The Beardsleyan Dandy: Icon of Grotesque Beauty
Abstract DANDYISM-the implicit doctrine of Oscar Wilde, James Abbott McNeill Whistler, and much of the Decadence-was the style of life Beardsley most admired, and of...
DANDY-WALKER SYNDROME;
DANDY-WALKER SYNDROME;
Introduction: Dandy-Walker Malformation is an inborn condition that includesthe triumvirate of cystic enlargement of the fourth ventricle, posterior fossa distension with riseof th...
Very early onset schizophrenia in Dandy-Walker variant: A case report
Very early onset schizophrenia in Dandy-Walker variant: A case report
The Dandy-Walker variant is a milder form of the Dandy-Walker Complex (DWC) with less severe radiological abnormalities. We describe a 13-year old girl with limited intellectual ca...
Regulation of mismatch repair protein MutSα functions by its Walker A and Walker B motifs
Regulation of mismatch repair protein MutSα functions by its Walker A and Walker B motifs
The mismatch recognition protein MutSα is an MSH2‐MSH6 heterodimer. Mismatch binding by MutSα triggers a series of downstream mismatch repair (MMR) reactions, including interacting...

Back to Top