Cerebellar hypoplasia


Cerebellar hypoplasia is characterized by reduced cerebellar volume, even though cerebellar shape is normal. It consists of a heterogeneous group of disorders of cerebellar maldevelopment presenting as early-onset non–progressive congenital ataxia, hypotonia and motor learning disability.
Various causes have been identified, including hereditary, metabolic, toxic and viral agents. It was first reported by French neurologist Octave Crouzon in 1929. In 1940, an unclaimed body came for dissection in London Hospital and was discovered to have no cerebellum. This unique case was appropriately named "human brain without a cerebellum" and was used every year in the Department of Anatomy at Cambridge University in a neuroscience course for medical students.
Cerebellar hypoplasia can sometimes present alongside hypoplasia of the corpus callosum or pons. It can also be associated with hydrocephalus or an enlarged fourth ventricle; this is called Dandy–Walker malformation.

Signs and symptoms

Non-progressive early onset ataxia and poor motor learning are the most common presentation.

Diagnosis

Magnetic resonance imaging

Three dimensional T2-weighted, axial, coronal, sagittal magnetic resonance imaging is considered appropriate for differentiation between gray matter and white matter acquisition of high-resolution anatomic information. T2w, axial and coronal imaging is more suitable for acquisition of high-resolution anatomic information and delineation of cortex, white matter, and gray matter nuclei. Diffusion tensor, axial imaging is used for evaluation of white matter microstructural integrity, identification of white matter tracts. CISS, axial + MPR imaging for evaluation of cerebellar folia, cranial nerves, ventricles, and foramina. Susceptibility weighted axial scans are employed for identification and characterization of hemorrhage, blood products, calcification, and iron accumulation.

Classification

Classification systems for malformations of the cerebellum are varied and are constantly being revised as greater understanding of the underlying genetics and embryology of the disorders is uncovered. A classification proposed by Patel S in 2002 divides cerebellar malformations in two broad groups: those with cerebellar hypoplasia and those with cerebellar dysplasia.

Treatment

There is no standard course of treatment for cerebellar hypoplasia. Treatment depends upon the underlying disorder and the severity of symptoms. Generally, treatment is symptomatic and supportive. Balance rehabilitation techniques may benefit those experiencing difficulty with balance.

Prognosis

The prognosis of this developmental disorder is highly based on the underlying disorder. Cerebellar hypoplasia may be progressive or static in nature. Some cerebellar hypoplasia resulting from congenital brain abnormalities/malformations are not progressive. Progressive cerebellar hypoplasia is known for having poor prognosis, but in cases where this disorder is static, prognosis is better.

History

Following clinical report by Crouzon in 1929 Sarrouy reported two pairs of siblings with congenital cerebellar hypoplasia in 1958. However pons, pyramidal tract and corpus callosum were also involved in these cases. Wichman et al. in 1985 reported three sibling pairs with congenital cerebellar hypoplasia : Mathews KD, in 1989 also reported two cases of cerebellar hypoplasia in a family with unaffected parents suggestive of autosomal recessive inheritance. The frequency and importance of the evaluation of the posterior fossa have increased significantly over the past 20 years owing to advances in neuroimaging with frequent reporting of posterior fossa malformation.