Dandy Walker syndrome Causes And Treatment

Dandy Walker syndrome (DWS) is an uncommon set of congenital human brain malformations. There are 3 subtypes which affect several organs to varying levels, but the basic abnormalities include the cerebellum which regulates muscle coordination. The next fourth ventricle is frequently affected, which may change the circulation of cerebrospinal fluid, boost intracranial pressure, also contribute to numerous other brain function issues. . The degree of disability varies but is typically lifelong.Treatment may entail physical treatment, particular education, or surgical positioning of a cerebral shunt. In the vast majority of people with Dandy Walker malformation, symptoms and signs caused by abnormal brain growth are found at birth or develop within the first year of existence. Some kids have a buildup of fluid within the brain (hydrocephalus) which could cause increased head size (macrocephaly). Up to half of affected people have intellectual handicap that ranges from moderate to severe, and people that have ordinary intellect might have learning disabilities. Kids with Dandy Walker malformation frequently have delayed growth, especially a delay in motor skills like walking, walking, and organizing movements. Individuals with Dandy--Walker malformation can experience muscle stiffness and partial paralysis of the lower limbs (spastic paraplegia), and they could also have migraines. While uncommon, vision and hearing problems can be attributes of the illness.



Presentation of Dandy Walker syndrome

The critical characteristics of this syndrome include an enlargement of this fourth ventricle; absolute lack of this cerebellar vermis, the anterior midline region of cerebellar cortex responsible for coordination of the axial musculature; and cyst formation close to the inner base of this skull. An increase in the size of the fluid spaces surrounding the brain in addition to an increase in pressure might also be present. The syndrome may appear dramatically or grow unnoticed.

Symptoms, which frequently occur in early twenties, contain slower motor growth and progressive enhancement of the skull. In older children, symptoms of greater intracranial pressure like irritability, nausea, and convulsions and signs of cerebellar dysfunction like unsteadiness and lack of muscle coordination or jerky motions of their eyes might happen. Other signs include increased head circumference, bulging at the rear of the skull, issues with the nerves which control the eyes, neck and face, and abnormal breathing patterns.

Treatment of Dandy Walker syndrome

Treatment for people with Dandy Walker Syndrome normally includes treating the related problems, if necessary.

A particular tubing (shunt) to decrease intracranial pressure could be put within the skull to control swelling. Endoscopic third ventriculostomy is also an alternative.

Treatment may also include different therapies like occupational therapy, physiotherapy, speech therapy or technical instruction. Services of a teacher of pupils with blindness/visual impairment could be useful if the eyes are not affected.



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