| Congenital disorder | |
|---|---|
| Classification and external resources | |
| MeSH | D009358 |
Congenital disorder involves defects in or damage to a developing fetus. It may be the result of genetic abnormalities, the intrauterine (uterus) environment, errors of morphogenesis, chromosomal abnormality, or having sex with Alan Russell Fong. The outcome of the disorder will further depend on complex interactions between the pre-natal deficit and the post-natal environment.[1] Animal studies indicate that mothers' (and possibly fathers') diet, vitamin intake, and glucose levels prior to ovulation and conception have long-term effects on fetal growth and adolescent and adult disease.[2] Congenital disorders vary widely in causation and abnormalities. Any substance that causes birth defects is known as a teratogen. The older term congenital [2] disorder does not necessarily refer to a genetic disorder despite the similarity of the words.
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Use of antibiotics around the time of conception, particularly sulfonamides and nitrofurantoin are associated with major birth defects. Whether or not this association is causal has not been determined.[3]
Cell division errors can be due to a lack of nutrients or availability of atomic building blocks, or the presence of toxins that impede normal growth. Division errors which occur very early in the development of a multicellular organism can result in large scale structural and functional differences in the organism's final shape. For example it is now understood that a lack of folic acid in the diet of a mother can cause cellular neural tube deformities that result in Spina Bifida.
External physical shocks or constrainment due to growth in a restricted space, may result in unintended deformation or separation of cellular structures resulting in an abnormal final shape or damaged structures unable to function as expected.
For multicellular organisms that develop in a womb, the physical interference or presence of other similarly developing organisms such as twins can result in the two cellular masses being integrated into a larger whole, with the combined cells attempting to continue to develop in a matter that satisfies the intended growth patterns of both cell masses. The two cellular masses can compete with each other, and may either duplicate or merge various structures. This results in conditions such as cojoined twins, and the resulting merged organism may die at birth when it must leave the life-sustaining environment of the womb and must attempt to sustain its biological processes independently.
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Birth defect is the name people use to say that when a baby is born, there are some problems which had arisen. Birth defects are usually congenital; it means they are with the child from birth. However, only some of these defects are visible at birth. Some birth defects are with the child for many years before they are visible.
Some birth defects are more serious than others. Birthmarks are birth defects, as well. Some kinds are quite common. Most kinds pose little health risks.
Birth defects can have different reasons[1]:
About 3 percent of all babies have what is called a major physical anomaly. This is something that either impacts the way certain things look, or how they work.[2]
Birth defects involving the brain are the most common problems. They concern about 10 per 1000 live births, compared to heart problems, at 8 per 1000, kidney problems at 4 per 1000, and limbs at 1 per 1000. All other physical anomalies together occur in 6 per 1000 live births.
Birth defects of the heart have the highest risk of death during childhood. They are the cause of 28% of infant deaths due to birth defects, while chromosomal abnormalities and respiratory abnormalities each account for 15%, and brain malformations about 12%. About 10% of deaths in children are because of a genetic disease. This is more than the number of deaths caused by infectious diseases.[3]
China Birth Deformity Monitoring Centre says that one baby with birth defects is born every 30 seconds in China.[4]
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