The cerebral palsy spectrum of disorders affects posture, muscle tone, and movement. The abnormal brain growth or damage that causes CP can occur before birth, during labor and delivery, in under a month of birth or during a child’s first few years of life while the child is young. Generally speaking, cerebral palsy results in movement impairment accompanied by heightened reflexes, flatness or stiffness of the legs and trunk, peculiar posture, involuntary motions, unstable walking, or some variation.

Cerebral palsy: A genetic disorder?

To better understand how DNA mutations, chromosomal deletions, hazards, and health status interact to provide direct paths toward abnormal cognitive development, researchers may now look at brain injury and brain deformity. This is made possible by the advent of neuroimaging technology. Scientists can now pinpoint Cerebral Palsy risk factors, mitigation strategies, and surgical approaches – thanks to studies. Understanding when, how, and why brain injury occurs during different phases of development is essential to reaching that aim. Numerous groups are working to minimize the prevalence of Cerebral Palsy. The sector has identified four key terms to assist in pinpointing “when” brain injury occurs.

  • Genetic proneness: Although Cerebral Palsy isn’t a genetic disease, researchers have found that some hereditary traits can increase a person’s risk of developing the disorder. A particular genetic condition does not directly cause cerebral palsy. However, genetic effects can have minor impacts on several genes. In addition, gene-to-gene interactions and complicated interactions with various environmental factors are possible outcomes of genetic impacts. This link often referred to as “complex breeding” or “multifaceted inheritance,” may explain the propensity for Cerebral Palsy to “run in the family” or, as the syndrome is clinically termed, “familial recurrence.” Premature birth, congenital malformations, pregnancy issues, hypertension, and other perinatal health disorders are a few that could be inherited.
  • Congenital cerebral palsy: While guardians get more educated about their child’s cerebral disorder, they discover that a child’s severity and cerebral palsy type can vary depending on brain damage. When a kid develops congenital cerebral palsy, it suggests that prenatal or postpartum circumstances may have contributed to the condition. Intrinsic brain impairment may not be identified right away, but it is a disorder that can be identified months or years after birth.

 Congenital cerebral palsy accounts for 70% of all diagnoses of the condition. Some causes of congenital disabilities include oxygen deprivation, complicated pregnancies, medical malpractice, preterm birth, low birth weight, growth restriction, sexual diseases, birth placement, foetal spasms, haemorrhages in the brain, poorly treated health problems, and exposure to toxins during critical developmental stages. Congenital cerebral palsy can also develop as a result of illnesses and fevers.

  • Acquired cerebral palsy: After birth, the brain continues to develop. Medical experts disagree about whether genetic cerebral palsy manifests at birth or within 28 days, while academics debate whether the brain develops fully within a couple of years. Understanding what caused it and when it occurred is essential to understanding the differences between congenital and acquired cerebral palsy. It is believed that in cases of inherited cerebral palsy, the kid was healthy at birth but suffered brain damage before the brain had fully developed. Nobody has developed cerebral palsy from birth. 10% of all diagnosed cases of cerebral palsy may be inherited. The actual cause of gained cerebral palsy is typically easier to identify than congenital cerebral palsy. Acquired cerebral palsy can be brought on by brain diseases, pneumococcal disease, viral encephalitis, mishaps, and injuries.
  • No CP: A case is labelled as having “No CP” if brain damage occurs after the brain has reached maturity, usually after a child turns five. Symptoms resembling cerebral palsy are recognized when there is no proof of the disorder. Still, an accident that affects the brain, such as head trauma or bloodstream infection, determines the cause.

Even though the situation is formally classified as No CP, the young child showing signs of cerebral palsy is treated as such. The term “No CP” now allows researchers to distinguish between occurrences of cerebral palsy that were formed after birth. In their research, some scholars fail to consider No CP situations.


Cerebral palsy can develop at birth or in the first few years of life. Many cerebral palsy patients can lead entire, independent lives with the correct diagnosis and care. However, cerebral palsy cannot always be avoided regardless of whether the mother follows the correct procedures. Talking to your doctor and beginning interventions as soon as possible are the most delicate things you can accomplish for an infant with cerebral palsy. One of the finest pediatric neurologists from Gurgaon in this field is Dr R.K Jain, whom you can consult if your kid suffers from an early stage of cerebral palsy.

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