Cockayne syndrome is a rare autosomal recessive dysmyelinating disease. Cockayne syndrome is classified among the childhood leukodystrophies, and brain imaging findings are cardinal features suggesting the diagnosis of Cockayne syndrome. Previously published Cockayne syndrome imaging studies have described major brain atrophy (predominantly white matter), bilateral and symmetrical calcifications, and a lack of myelination of the white matter, but whether these findings are due to hypomyelination or demyelination remains unclear.
The diagnosis is considered very likely if the first 2 clinical criteria and at least 3 of the other criteria mentioned above are present.
Cockayne syndrome is one of the causes of basal ganglia calcifications in a child. Calcification may also occur in cerebellar and cerebral cortical regions. CT may also show early atrophy.
There is atrophy which predominantly involves the supratentorialwhite matter, the cerebellum, the corpus callosum, and the brainstem .
- T2: calcification may be seen as low signal in putaminal (most common), dentate nuclear and cortical regions
The combination of demyelination and basal ganglia calcification may, therefore, be helpful in the imaging of this entity .
History and etymology
This condition is named after Edward Alfred Cockayne, English physician (1880-1956).
- Pelizaeus-Merzbacher: may show similar features in early stages, but no calcification occurs
- Mitochondrial diseases: the severe and progressive brain atrophy is more suggestive of Cockayne syndrome
- congenital cytomegalovirus infections: brain calcifications typically show a periventricular subependymal distribution
- Aicardi-Goutières syndrome: calcifications punctuate in basal ganglia, deep and periventricular white matter