There is no standard course of treatment for cerebellar hypoplasia.

Cerebellar hypoplasia is particularly common in cats and has similar symptoms.

The first known case of cerebellar hypoplasia was discovered in the year of 1940.

In addition, type 1 lissencephaly is closely associated with cerebellar hypoplasia.

Cerebellar hypoplasia may be progressive or static in nature.

If a cat is exposed during pregnancy, the virus can cause cerebellar hypoplasia in her offspring.

Infection of the cat fetus and kittens less than two weeks old causes cerebellar hypoplasia.

Cerebellar hypoplasia causes jerky movements, tremors and generally uncoordinated motion.

Some cerebellar hypoplasia resulting from congenital brain abnormalities/malformations are not progressive.

In mild to moderate cases the pups can be born with neurological abnormalities such as cerebellar hypoplasia.

Patients have cerebellar hypoplasia and suffer from congenital lymphedema and hypotonia.

Less severe cases with isolated cerebellar hypoplasia and symptoms of ataxia and jitteriness have been reported occasionally.

Mink enteritis virus is similar in effect to feline panleukopenia, except that it does not cause cerebellar hypoplasia.

Cerebellar hypoplasia is a disorder found in cats and dogs in which the cerebellum is not completely mature at birth.

Usually symptoms of cerebellar hypoplasia can be seen immediately at birth in cats, but sometimes can take two months or so to become apparent in dogs.

Cerebellar hypoplasia may be caused by thyroid abnormalities, environmental influences such as drugs and chemicals or viral infections or stroke.

The brain impairments include cerebellar hypoplasia, mild cerebral cortex atrophy and a reduced corpus callosum.

Cerebellar hypoplasia is a rare embryonic developmental disorder in which the cerebellum is either missing entirely or is smaller than usual.

Progressive cerebellar hypoplasia is known for having poor prognosis, but in cases where this disorder is static, prognosis is better.

Cerebellar abiotrophy in horses was originally thought to be a form of cerebellar hypoplasia and was described as such in older research literature.

VLDLR-associated cerebellar hypoplasia See for a review:

Mutations of this gene may lead to a variety of symptoms and diseases, which include type I lissencephaly, cerebellar hypoplasia, and atherosclerosis.

It is a rare condition, characterized by cardiac malformation (heart defects), cerebellar hypoplasia and cranial dysmorphism (symptoms involving the brain).

She presented with IUGR, colitis, immune deficiency, cerebellar hypoplasia, microcephaly and very short telomeres.

The most prominent of these diseases are type I lissencephaly, VLDR-associated cerebellar hypoplasia, and atherosclerosis.