Cerebellar hypoplasia

Below you will find more information about Cerebellar hypoplasia from Medigest. If you believe that you are suffering from any of the symptoms of Cerebellar hypoplasia it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Cerebellar hypoplasia and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Cerebellar hypoplasia comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.


Cerebellar hypoplasia is a condition which affects the development of the cerebellum. The developmental problem actually results in an underdeveloped cerebellum, smaller than usual in size. Cerebellar hypoplasia may result because of genetics, or can also occur sporadically. The condition is associated with other diseases such as the Walker-Warborg syndrome, Dandy Walker Syndrome, and the Werdnig-Hoffman Syndrome.


Although there is no treatment to cure a patient with cerebellar hypoplasia, the treatment given is supportive in nature and can help make living with the condition easier for the patient and family.

Symptoms and Signs

Symptoms of cerebellar hypoplaxia differs with infants and children, and with older children. In infants, the symptoms are commonly unhealthy muscle tone, problems with speech and development, seizures, balance and walking problems, mental retardation, and involuntary movement of the eyes. Older children exhibit symptoms such as hearing impairment, clumsiness, dizzy spells, and headaches.


Genetics, thyroid problems, or environmental factors can cause cerebellar hypoplasia. Among environmental factors are drugs, viral infections, chemicals, or even strokes.

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