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Precision Medicine
4 May 2021
It is a neurological malformation in which the baby has a significant reduction in the size of the head compared to normal dimensions at that stage of life.
If detected at birth, it is likely due to abnormal brain growth in the gestation process, or if identified later, it is the result of poor development during infancy in which the head simply stops growing.
Microcephaly is a condition that can be due to various genetic and environmental factors, as well as:
The characteristic symptoms consist of:
Potential risks:
Depending on the origin and seriousness of microcephaly, the following may occur:
Once the specialist performs a physical examination and analyzes the family medical history, they will measure the baby’s head to compare it with a growth chart, making timely follow-ups.
You may also decide to measure the parent’s head to establish if it is due to a family trait. If your child has been developmentally impaired, the doctor will most likely order blood, urine, and genetic tests, as well as imaging studies such as MRI and CT scans, in order to establish the cause of the delay.
If your child suffers from craniosynostosis, they will perform surgery to correct the anomaly, but in other cases, there is no therapy that solves the problems caused by microcephaly, so the treatment will focus on achieving control of the condition through various support programs, such as speech and occupational therapy, as well as physiotherapy, which will seek to give the child a better quality of life.
If there are convulsive or hyperactive episodes, they can be treated with different drugs.
At the Neurological Center, a select group of highly trained and certified doctors in the various neurological specialties are ready to assist you with the quality and warmth that characterizes us.
Nervous system specialties
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