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Susceptibility to teratogenesis varies with the developmental stage at the time of exposure to an adverse influence. There are critical periods of susceptibility to agents and organ systems affected by these agents. Teratogenic agents act in specific ways on developing cells and tissues to initiate sequences of abnormal developmental events.
Toxic substances that are capable of causing structural congenital abnormalities can be termed teratogens. [4] They are agents extrinsic to embryo or fetus which exert deleterious effects leading to increased risk of malformation, carcinogenesis, mutagenesis, altered function, deficient growth or pregnancy wastage. [5]
The effect of the developmental toxicants depends on the type of substance, dose, duration, and time of the exposure. The first few weeks of embryogenesis in humans is more susceptible to these agents. The embryogenesis is the most crucial time for the action of any teratogenic substances to result in birth defects.
Teratogens are substances that may cause birth defects via a toxic effect on an embryo or foetus. Wikimedia Commons has media related to Teratogens . See also the categories Carcinogens and Mutagens
Susceptibility to teratogenesis varies with the developmental stage at the time of exposure to an adverse influence. There are critical periods of susceptibility to agents and organ systems affected by these agents. Teratogenic agents act in specific ways on developing cells and tissues to initiate sequences of abnormal developmental events.
The international pictogram for chemicals that are sensitising, mutagenic, carcinogenic or toxic to reproduction. Reproductive toxicity refers to the potential risk from a given chemical, physical or biologic agent to adversely affect both male and female fertility as well as offspring development. [1]
A toxic injury is a type of injury resulting from exposure to a toxin.Toxic injuries can manifest as teratogenic effects, respiratory effects, gastrointestinal effects, cardiovascular effects, hepatic effects, renal effects, neurological effects, or a combination thereof.
The (R)-enantiomer has the desired sedative effect while the (S)-enantiomer harbors embryo-toxic and teratogenic effects. Attempting to extract solely R-thalidomide does not remove the risk of birth defects, as it was demonstrated that the "safe" R-thalidomide undergoes an in vivo chiral inversion to the "teratogenic" S-thalidomide.