These threats all effect the development of a baby’s immune system during both the prenatal and neonatal stages of development (Wigle, 2003). Ultraviolet light and ionizing radiation are both types of radiation (EPA, n.d.). Exposure mainly comes from black lights, tanning beds and x-rays. (EPA, n.d.). TCDD is a by-product of the incomplete combustion of fossil fuels, wood and chlorinates organic chemicals. Exposure mainly comes from meat, dairy products and fish (EPA, n.d.).When babies are exposed, these environmental threats can interfere with hematopoietic cell proliferation, differentiation, migration, expansion of lineage-committed stem cells, colonization of postnatal lymphopoietic compartments, cell-to-cell interactions, and maturation of immune-competence. Also, if babies are exposed to ionizing radiation between 10-17 gestational weeks, the threat can cause microcephaly (Etzel & Balk, 2003). When scientists tested these environmental threats on rodents, the animals had an increased risk of hypersensitivity and autoimmune diseases (Wigle, 2003). There is little evidence that proves these environmental threats effect humans in the same way (Wigle,
These threats all effect the development of a baby’s immune system during both the prenatal and neonatal stages of development (Wigle, 2003). Ultraviolet light and ionizing radiation are both types of radiation (EPA, n.d.). Exposure mainly comes from black lights, tanning beds and x-rays. (EPA, n.d.). TCDD is a by-product of the incomplete combustion of fossil fuels, wood and chlorinates organic chemicals. Exposure mainly comes from meat, dairy products and fish (EPA, n.d.).When babies are exposed, these environmental threats can interfere with hematopoietic cell proliferation, differentiation, migration, expansion of lineage-committed stem cells, colonization of postnatal lymphopoietic compartments, cell-to-cell interactions, and maturation of immune-competence. Also, if babies are exposed to ionizing radiation between 10-17 gestational weeks, the threat can cause microcephaly (Etzel & Balk, 2003). When scientists tested these environmental threats on rodents, the animals had an increased risk of hypersensitivity and autoimmune diseases (Wigle, 2003). There is little evidence that proves these environmental threats effect humans in the same way (Wigle,