Microcephaly (my-kro-SEF-ah-lee) is a rare condition in which a child's brain
does not fully develop, resulting in an abnormally small head size.
More to Know
Microcephaly, which can be passed down through families, can be present at birth
or develop during the first 2 years of life. Chromosomal disorders (such as Down
syndrome), metabolic disorders, bacterial meningitis,
and lack of oxygen all can cause microcephaly. A baby is at increased risk if the
mother used drugs or alcohol during her pregnancy or was exposed to chemicals, radiation,
or certain viruses.
Some children with microcephaly will have no symptoms or developmental delays,
and will be generally unaffected. Others will have varying degrees of developmental
problems depending on what caused the microcephaly. They may have intellectual disabilities,
delayed speech and
motor functions, vision and hearing problems, dwarfism
or short stature, seizures,
or other problems associated with brain abnormalities.
Keep in Mind
There is no treatment for microcephaly that can reverse the problem. Children who
have it can, however, benefit from early intervention programs with physical,
and speech therapists
to help them reach their full potential and enhance their quality of life.
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