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About 3% of newborns have a "major physical anomaly", meaning a physical anomaly that has cosmetic or functional significance.<ref>Kumar, Abbas and Fausto, eds., ''Robbins and Cotran's Pathologic Basis of Disease, 7th edition'', p.470.</ref>
About 3% of newborns have a "major physical anomaly", meaning a physical anomaly that has cosmetic or functional significance.<ref>Kumar, Abbas and Fausto, eds., ''Robbins and Cotran's Pathologic Basis of Disease, 7th edition'', p.470.</ref>

=== Teratogenic agents ===
A wide range of different chemicals and environmental factors are suspected or are known to be teratogenic in humans and in animals. A selected few include:

*Drugs and medications: [[alcohol]] ([[ethanol]]) (see [[fetal alcohol spectrum disorder]]), [[isotretinoin]] (13-cis-retinoic acid, Roaccutane), [[temazepam]] (Restoril; Normisson), [[nitrazepam]] (Mogadon), [[nimetazepam]] (Ermin), [[aminopterin]] or [[methotrexate]], [[androgenic|androgenic hormones]], [[busulfan]], [[captopril]], [[enalapril]], [[coumarin]], [[cyclophosphamide]], [[diethylstilbestrol]], [[phenytoin]] (diphenylhydantoin, Dilantin, Epanutin), Dexamethasone, [[etretinate]], [[lithium]], [[methimazole]], [[penicillamine]], [[tetracyclines]], [[thalidomide]], [[trimethadione]], methoxyethyl [[ethers]], [[Flusilazole]], [[valproic acid]], and many more.
*Environmental chemicals: [[polycyclic aromatic hydrocarbons]] (polynuclear aromatic hydrocarbons), [[polychlorinated biphenyl]]s (PCBs), [[polychlorinated dibenzodioxins]] a.k.a dioxin, [[polychlorinated dibenzofurans]] (PCDFs), [[hexachlorobenzene]] [[hexachlorophene]], [[mercury (element)|organic mercury]], [[ethidium bromide]], etc.
*Ionizing radiation:{{Citation needed|date=April 2013}} [[atomic weapons]] fallout ([[iodine-131]], [[uranium]]), [[background radiation]], diagnostic [[x-ray]]s, [[radiation therapy]]{{citation needed|date=April 2013}}
*Infections: [[cytomegalovirus]], [[herpes virus]], [[parvovirus B19]], [[rubella|rubella virus]] (German measles), [[syphilis]], [[toxoplasmosis]], [[Venezuelan equine encephalitis virus]]. (An easy way to remember maternal infections is TORCH: Toxoplasmosis, Other agents, Rubella, CMV and HSV.)
*Metabolic imbalance: [[alcoholism]], [[cretinism|endemic cretinism]], [[diabetes]], [[folic acid deficiency]], [[iodine deficiency]], [[hyperthermia]], [[phenylketonuria]], [[rheumatic disease]] and [[heart block|congenital heart block]], [[Virilization|virilizing tumors]]

The status of some of the above substances (e.g. diphenylhydantoin) is subject to debate, and many other compounds are under varying degrees of suspicion. These include [[Agent Orange]],<ref name="pmid6137083">{{cite journal |author=Linnainmaa K |title=Sister chromatid exchanges among workers occupationally exposed to phenoxy acid herbicides 2,4-D and MCPA |journal=Teratog., Carcinog. Mutagen. |volume=3 |issue=3 |pages=269–79 |year=1983 |pmid=6137083|doi=10.1002/1520-6866(1990)3:3<269::AID-TCM1770030306>3.0.CO;2-F}}</ref> [[nicotine]],<ref name="pmid15033289">{{cite journal |author=Vaglenova J, Birru S, Pandiella NM, Breese CR |title=An assessment of the long-term developmental and behavioral teratogenicity of prenatal nicotine exposure |journal=Behav. Brain Res. |volume=150 |issue=1-2 |pages=159–70 |year=2004 |pmid=15033289|doi=10.1016/j.bbr.2003.07.005}}</ref> [[aspirin]] and other [[NSAID]]s. Other compounds are known as severe teratogens based on veterinary work and animal studies, but aren't listed above because they have not been studied in humans, e.g. [[cyclopamine]]. Teratogenic effects also help to determine the [[pregnancy category]] assigned by regulatory authorities; in the United States, a pregnancy category of X, D, or C may be assigned if teratogenic effects (or other risks in pregnancy) are documented or cannot be excluded.


==Other animals==
==Other animals==

Revision as of 00:14, 22 November 2013

A two-headed calf
A grown steer with five legs.

Teratology is the study of abnormalities of physiological development. It is often thought of as the study of human congenital abnormalities, but it is much broader than that, taking in other non-birth developmental stages, including puberty; and other non-human life forms, including plants. The related term developmental toxicity includes all manifestations of abnormal development by toxic substances. These may include growth retardation, delayed mental development or other congenital disorders without any structural malformations.[1]

Etymology

The term stems from the Greek τέρας teras (genitive τέρατος teratos), meaning 'monster' or 'marvel', and λόγος logos, meaning 'the word' or, more loosely, 'the study of'.[2]

As early as the 17th century, teratology referred to a discourse on prodigies and marvels of anything so extraordinary as to seem abnormal. In the 19th century, it acquired a meaning more closely related to biological deformities, mostly in the field of botany. Currently, its most instrumental meaning is that of the medical study of teratogenesis, congenital malformations or individuals with significant malformations. There are many pejorative terms that have historically been used to describe individuals with significant physical malformations. The term was popularized in the 1960s by Dr. David W. Smith of the University of Washington Medical School, one of the researchers who became known in 1973 for the discovery of Fetal alcohol syndrome.[3] With greater understanding of the origins of birth defects, the field of teratology now overlaps with other fields of basic science, including developmental biology, embryology, and genetics.

Mammalia

Teratogenesis

Along with this new awareness of the in utero vulnerability of the developing mammalian embryo came the development and refinement of The Six Principles of Teratology which are still applied today. These principles of teratology were put forth by Jim Wilson in 1959 and in his monograph Environment and Birth Defects.[4] These principles guide the study and understanding of teratogenic agents and their effects on developing organisms:

  1. Susceptibility to teratogenesis depends on the genotype of the conceptus and the manner in which this interacts with adverse environmental factors.
  2. 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.
  3. Teratogenic agents act in specific ways on developing cells and tissues to initiate sequences of abnormal developmental events.
  4. The access of adverse influences to developing tissues depends on the nature of the influence. Several factors affect the ability of a teratogen to contact a developing conceptus, such as the nature of the agent itself, route and degree of maternal exposure, rate of placental transfer and systemic absorption, and composition of the maternal and embryonic/fetal genotypes.
  5. There are four manifestations of deviant development (Death, Malformation, Growth Retardation and Functional Defect).
  6. Manifestations of deviant development increase in frequency and degree as dosage increases from the No Observable Adverse Effect Level (NOAEL) to a dose producing 100% Lethality (LD100).

Studies designed to test the teratogenic potential of environmental agents use animal model systems (e.g., rat, mouse, rabbit, dog, and monkey). Early teratologists exposed pregnant animals to environmental agents and observed the fetuses for gross visceral and skeletal abnormalities. While this is still part of the teratological evaluation procedures today, the field of Teratology is moving to a more molecular level, seeking the mechanism(s) of action by which these agents act. Genetically modified mice are commonly used for this purpose. In addition, pregnancy registries are large, prospective studies that monitor exposures women receive during their pregnancies and record the outcome of their births. These studies provide information about possible risks of medications or other exposures in human pregnancies.

Understanding how a teratogen causes its effect is not only important in preventing congenital abnormalities but also has the potential for developing new therapeutic drugs safe for use with pregnant women.

Humans

In humans, congenital disorders resulted in about 510,000 deaths globally in 2010.[5]

About 3% of newborns have a "major physical anomaly", meaning a physical anomaly that has cosmetic or functional significance.[6]

Other animals

Fossil record

Evidence for congenital deformities found in the fossil record is studied by paleopathologists, specialists in ancient disease and injury. Fossils bearing evidence of congenital deformity are scientifically significant because they can help scientists infer the evolutionary history of life's developmental processes. For instance, because a Tyrannosaurus rex specimen has been discovered with a block vertebra, it means that vertebrae have been developing the same basic way since at least the most recent common ancestor of dinosaurs and mammals. Other notable fossil deformities include a hatchling specimen of the bird-like dinosaur, Troodon, the tip of whose jaw was twisted.[7] Another notably deformed fossil was a specimen of the choristodere Hyphalosaurus, which had two heads- the oldest known example of polycephaly.[8]

Plantae

In botany, teratology investigates the theoretical implications of abnormal specimens. For example, the discovery of abnormal flowers—for example, flowers with leaves instead of petals, or flowers with staminoid pistils—furnished important evidence for the "foliar theory", the theory that all flower parts are highly specialised leaves.

See also

References

  1. ^ Rogers, J.M., Kavlock, R.J. Developmental toxicology. In C.D. Klaassen (ed.): Casarett & Doull's Toxicology, 5th ed. pp. 301-331. McGraw-Hill, New York, 1996. ISBN0-07-105476-6.
  2. ^ "Online Etymology Dictionary". http://www.etymonline.com/index.php?term=logos. {{cite web}}: |access-date= requires |url= (help); Check date values in: |accessdate= (help); External link in |work= (help); Missing or empty |url= (help)
  3. ^ Jones K.L., Smith D.W, Ulleland C.N., Streissguth A.P. (1973). "Pattern of malformation in offspring of chronic alcoholic mothers". Lancet. 1 (7815): 1267–1271. doi:10.1016/S0140-6736(73)91291-9. PMID 4126070.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ James G. Wilson, (1973). Environment and Birth Defects (Environmental Science Series). London: Academic Pr. ISBN 0-12-757750-5.{{cite book}}: CS1 maint: extra punctuation (link)
  5. ^ Lozano, R (2012 Dec 15). "Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010". Lancet. 380 (9859): 2095–128. PMID 23245604. {{cite journal}}: Check date values in: |date= (help)
  6. ^ Kumar, Abbas and Fausto, eds., Robbins and Cotran's Pathologic Basis of Disease, 7th edition, p.470.
  7. ^ Molnar, R. E., 2001, Theropod paleopathology: a literature survey: In: Mesozoic Vertebrate Life, edited by Tanke, D. H., and Carpenter, K., Indiana University Press, p. 337-363.
  8. ^ Ji Q., Wu, X.-C. and Cheng, Y.-N. (2010). "Cretaceous choristoderan reptiles gave birth to live young." Naturwissenschaften, 97(4): 423-428. doi:10.1007/s00114-010-0654-2

External links