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Is there any treatment?
There is no treatment for microcephaly that can return a child’s head to a normal size or shape. Treatment focuses on ways
to decrease the impact of the associated deformities and neurological disabilities. Children with microcephaly and developmental
delays are usually evaluated by a pediatric neurologist and followed by a medical management team. Early childhood intervention
programs that involve physical, speech, and occupational therapists help to maximize abilities and minimize dysfunction. Medications
are often used to control seizures, hyperactivity, and neuromuscular symptoms. Genetic counseling may help families understand
the risk for microcephaly in subsequent pregnancies
What is the prognosis?
Some children will only have mild disability. Others, especially if they are otherwise growing and developing normally, will
have normal intelligence and continue to develop and meet regular age-appropriate milestones.
What research is being done?
The National Institute of Neurological Disorders and Stroke (NINDS) conducts research relating to microcephaly in its laboratories
at the National Institutes of Health (NIH) and supports additional research through grants to major medical institutions across
the country. A small group of researchers studying a rare neurometabolic syndrome (3-PGDH), which causes microcephaly, have
successfully used amino acid replacement therapy to reduce and prevent seizures.