Causes
ALL is a type of cancer that is caused by variations in genes. If a portion of a gene is damaged, broken, mutated, or deleted, it is possible to develop ALL.
Some of the genetic changes from this cancer are inherited and are found in a child from birth. However, in most cases, ALL occur in a child after birth due to genetic changes. These are the genetic changes that are then mutated and passed down the lineage. TA genetic condition that increases the risk to ALL includes the following:
Down syndrome
Fanconi anemia
Li-Fraimeni syndrome
Bloom syndrome
Kleinfelter syndrome
Neurofibromatosis.
The factors that develop these genetic changes are not completely known and these factors most likely affect young adults rather than individuals in their childhood ages.
Factors that cause genetic damage and case mutation are the following:
-Radiation exposure.
-Exposure to harmful chemicals like benzene.
-Infection by human T lymphoma HTLV-1 or Epstein Barr Virus.
Upon successful elimination of risk factors of ALL, the probability of developing this disease decreases but it is impossible to completely prevent this disease.
Most individuals with ALL do not show any risk factor and there is no way to know the full cause of ALL in an individual.