Lissencephaly is a rare, gene linked malformation of the brain in which the normal convolutions in the cerebral cortex are missing and is characterised by an abnormally small head. Children with usual condition of lissencephaly have normal sized head at birth while the reduced size of head occurs in micorlissencephaly.
It occurs due to the migration of defective neuronal during embryonic development. It involves transportation of nerve cells to their permanent position from their place of origin.
Some common symptoms of this condition include:
Although there is no cure for lissencephaly, but the children may show progress in development over time. Supportive care should be given to provide comfort and help in feeding and other needs. Seizure may cause problems but anticonvulsant medications may provide relief.
Recent researches on lissencephaly have identified the genes which are responsible for this condition. These researches have laid the foundation for developing effective treatment and measures for neuronal migration disorder.
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Read more article on Understand Lissencephaly
The prognosis for children with lissencephaly depends on the degree of brain malformation, early diagnosis, and early therapy.read more
Lissencephaly is a rare, gene-linked brain malformation characterized by the absence of normal convolutions in the cerebral cortex.read more