Info on Schizencephaly
Schizencephaly
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ORDR lists rare diseases for information purposes only and does not guarantee that a condition is rare. Read moreThe links on this page may take you to sites outside of the NIH. (See Disclaimer for details.)
Schizencephaly is a developmental birth defect. It is characterized by abnormal slits or clefts in the cerebral hemispheres of the brain. People with clefts in both hemispheres commonly have developmental delays, delays in speech and language skills, seizures, and problems with brain-spinal cord communication. Individuals with clefts in only one hemisphere are often paralyzed on one side of the body, may have seizures, and may have average to near-average intelligence. Other signs and symptoms may include an abnormally small head (microcephaly), hydrocephalus, intellectual disability, partial or complete paralysis, or poor muscle tone (hypotonia). Treatment generally consists of physical therapy and drugs to prevent seizures. In cases that are complicated by hydrocephalus, a surgically implanted tube, called a shunt, is often used to divert fluid to another area of the body where it can be absorbed.[1]
References
- NINDS Schizencephaly Information Page. NINDS. May 6, 2010 Available at: http:/
/ www.ninds.nih.gov/ disorders/ schizencephaly/ schizencephaly.htm. Accessed September 28, 2011.
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