Colpocephaly is a congenital brain abnormality in which the occipital horns – the posterior or rear portion of the lateral ventricles (cavities) of the brain — are larger than normal because white matter in the posterior cerebrum has failed to develop or thicken.
Although the cause of colpocephaly is unknown, researchers believe that the disorder results from some kind of disturbance in the fetal environment that occurs between the second and sixth months of pregnancy.
Colpocephaly, one of a group of structural brain disorders known as cephalic disorders, is characterized by microcephaly (an abnormally small head) and mental retardation. Other features may include:
- Movement abnormalities
- Muscle spasms
Colpocephaly may be diagnosed late in pregnancy, although it is often misdiagnosed as hydrocephalus (excessive accumulation of cerebrospinal fluid in the brain). It may be more accurately diagnosed after birth when signs of mental retardation, microcephaly, and seizures are present.
The prognosis for individuals with colpocephaly depends on the severity of the associated conditions and the degree of abnormal brain development.
There is no definitive treatment for colpocephaly. Anticonvulsant medications are often prescribed to prevent seizures, and doctors rely on exercise therapies and orthopedic appliances to reduce shrinkage or shortening of muscles. Some children benefit from special education.