What Is Microcephaly?
During pregnancy, the size of the baby’s head depends on the growth of the brain. When the brain stops growing, it hampers the development of the skull causing comparatively smaller head size. Microcephaly is the birth defect either seen as an isolated condition or along with other birth defects. The development of the brain during pregnancy is sometimes normal, but due to some trauma or damage, the development process is interrupted. Microcephaly is rare, occurring in 2 to 12 babies per 10,000 births. The condition is often congenital (by birth), but also there are chances of children developing it at a later age.
What Are the Causes of Microcephaly?
The size of the baby’s skull grows with the size of his brain. What causes this condition is still unknown. However, there are some condition that affects the development of the brain, such as;
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Down Syndrome:
It is a chromosomal condition that occurs due to an extra pair of chromosome 21 in the baby’s genes. It is responsible for the development of the baby’s brain and body, and the condition causes distinct facial features, intellectual disabilities, or physical problems in the child.
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Prenatal Viral Infections:
Viral infections like zika virus, rubella, toxoplasmosis, or cytomegalovirus can play a major role in this condition.
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Alcoholism During Pregnancy:
When a mother is addicted to substance abuse, there are more chances of a child having birth defects like this.
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Gestational Diabetes:
Owing to hormonal changes during pregnancy, sugar level rises, which cause pregnancy-related diabetes. However, with proper diet, exercise and medication, this can be managed.
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Metal Poisoning:
There are metals like mercury that cause metal poisoning, in turn causing birth defects in the child.
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Malnutrition in Mother:
Diet plays an important role during pregnancy, not only for children but also for mothers. There are a plethora of conditions that can be managed just by balancing the diet of the pregnant mother.
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Genetic Mutation:
Genes that are passed from biological parents play a major role in the embryo’s body formation in the mother’s womb. When there are changes in genes in an embryo, there are higher chances of birth-related defects in children, and one of the defects is microcephaly.
Untreated phenylketonuria (PKU) is another inherited genetic mutation that is caused when the body is unable to break down an amino acid called phenylalanine.
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Brain Problems:
Complications during birth, like lack of oxygen to the newborn, can cause injury to the brain, and this can cause many fatal conditions to the child.
What Are the Signs and Symptoms Associated With Microcephaly?
Besides the distinctly identifiable smaller head, there are other symptoms of microcephaly. They are as follows:
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Problems related to eyesight and hearing.
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Seizures.
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Poor appetite.
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High pitched cry.
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Developmental delays like delayed speech and walking.
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Trouble in learning.
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Abnormal muscle tone.
How to Diagnose Microcephaly?
If a mother is going for regular checkups, there are chances that the doctor will detect any birth defect before the birth, during a prenatal ultrasound in the late second trimester or third trimester. Besides, if the condition is developed after birth, the pediatrician will detect it during regular checkups while measuring the circumference of the baby’s head, or complete physical examination with the prenatal birth history of a child. Likewise, obtaining regular milestones while growing up, such as crawling or walking, or speaking the first word, is another measure for checking for any intellectual disabilities. Also, the appearance of a head after birth, high-pitched crying, feeding difficulties, and muscle spasms are external signs that this condition shows.
If a baby is showing any above symptoms while growing up, healthcare providers may suggest for following tests:
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Computed tomography scan (CT scan).
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X-rays.
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Magnetic resonance imaging scan (MRI scan).
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Blood testing.
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Genetic testing.
What Are the Complications of Microcephaly?
Sometimes there are no other complications in a little one except for the small head, but there are chances of some complications like:
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Congenital Zika Syndrome: It is caused by the zika virus. It is a bunch of congenital abnormalities affecting the fetus.
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Cerebral Palsy: Cerebral Palsy is a birth defect caused by abnormal brain development. The result of this syndrome is a defect in muscle tone, movement, and posture of the body.
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Dwarfism: It is a genetic mutation that affects the growth of the bones in the body. This disorder creates shortness of height. Moreover, people with this syndrome are often seen with hunched back and bowed legs.
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Face Deformities: Due to an abnormally small head, facial features are also affected.
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Seizures: Due to an abnormally smaller-sized head, there are chances of developmental defects of the brain. The deformity related to the brain results in uncontrolled electrical disturbances. The severity of this condition can also cause loss of consciousness in children.
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Other Problems: Problems with vision, hearing, speech, and walking.
What Is the Treatment for Microcephaly?
Although there is no known cure for the condition, according to severity, the symptoms or complications can be managed. Babies with mild microcephaly might not require any treatment, but a severe condition associated with the brain does require treatment measures, such as speech therapy, occupational therapy, physical therapy, or drug therapy.
Pregnant women should be educated about the importance of diet during and after pregnancy. Additionally, mothers addicted to drugs, smoking, or alcohol should go for rehabilitation therapy before conceiving or at least give their detailed history to the doctor.
Conclusion
Microcephaly is a birth defect caused by many syndromes. The defect results in an underdeveloped skull and brain. Although there are no known treatments available to cure the condition, the symptoms or complications associated with it can be managed. Parents and doctors are required to give extra attention to the care of the patient.
