Birth defect
condition present at birth regardless of cause; human disease or disorder developed prior to birth From Wikipedia, the free encyclopedia
A birth defect (or congenital disorder) is a defect in a baby at birth, or which develops in the first month of life (as an embryo)[2] or in pregnancy.
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The term is neutral as to whether the cause is genetic (inherited birth defect) or environmental (causes in the environment, that is, outside the foetus). If a condition is congenital, that is neutral language. Often it is not known what causes a condition found at birth. In common use, it is referred to as a birth defect. The term is also neutral as to cause.
Hereditary disease (inherited) is a type of genetic disorder, or birth defect. These come from family, and can be done while the body is making the right sequences of DNA. Conditions might also happen from genetic disorder if it is making the wrong instructions in development. However if it is because of genetics the instructions for making the DNA from the parents lead to the hereditary disease. They can also be passed down via the X chromosome, which are called X-linked genetic disorders. If the parents are siblings, bad parts (traits) of the two people might not get cancelled out. The distance between genes on the DNA determines how easily they may break or be wrong,[verification needed] which affects development and reproduction during conception and in cell division phase. When the sperm is in the egg and beginning to form, errors can happen by accident, and sometimes do not get caught, leading to a disorder. When errors form from parents, and the DNA is made correctly, errors can happen. Errors can come from duplicate[verification needed] or recursive genes, such as when both parents are siblings.
Genetic abnormalities, which are hereditary, are one cause. Other types be caused by conditions (such as infectious diseases) which a baby may get.[3] However, it may not be known what caused the condition. Sometimes doctors may find out that a baby has a congenital disorder before its birth. They use prenatal diagnosis and screening tests, such as amniocentesis.[4] Some test are for the dormant genes. Tests for recessive genetic conditions or disease, where the parents do not show the signs of a condition, or for dominant genes where there might be something inheritable the family history, for example. People might check because their parents or grandparents had a disease. Many conditions cause people to become infertility, such as Down syndrome and Cystic Fibrosis (CF).
Genetic defects
Lethal or damaging genes
Some gene alleles (versions of a gene) can damage the fetus.
Conditions like dwarfism are nearly always genetic in origin. One type, achondroplasia, happens when a child's bones does not grow correctly. Another type is caused by pituitary malfunction, where the pituitary gland, which puts out growth hormones, does not work properly.[5]
Many genetic disorders are caused by mutations (or changes) in gene alleles. Mutations can cause development to go wrong, or a simple biochemical deficiency (the body does not have enough of an important chemical). In the case of a chemical deficiency, the problem may be curable. For example, phenylketonuria was a cause of mental retardation. Doctors came up with a simple test to find which babies have this condition. They found that if these children got treated and followed a strict diet, they could get enough of the chemical they needed. Phenylketonuria now causes few cases of mental retardation.
Chromosomes
Cells divide and copy themselves to produce gametes. Sometimes, errors happen in the way that chromosomes are copied during this process. These errors are then copied again and again as cells keep dividing and copying themselves. The most common chromosomal disorder is Down syndrome (historically 'Mongolism'). This condition happens when a child has three copies of the 21st chromosome, instead of two.
Maternal environment
Infectious diseases
The other main type of congenital disorder is caused by an infectious disease being passed from mother to child. For example, If a pregnant woman gets rubella, her child can have many birth defects. Congenital syphilis was common a century ago, and congenital AIDS occurs today, and is common in some parts of Africa.
Screening and antibiotics has caused the number of infections transmitted by the mother to drop. It is a much smaller proportion than a century ago, despite AIDS. Also, maternal nutritional defects are much rarer, except in countries where food supply is limited. Therefore, genetic disorders have grown as a proportion of the total congenital defects.
Substances taken by the mother
Chemicals
Sometimes mothers take chemicals which cause the embryo damage.[6] Any substance that causes birth defects is known as a teratogen.
Drugs taken by the mother may affect development of the embryo. Pregnant women are not allowed to use some drugs. For example, thalidomide should not be used by a pregnant woman, or it can cause many defects in the foetus.
Lifestyle
If the mother took certain things during pregnancy, these can lead to problems with the baby. Common examples of such things are smoking tobacco, or drinking alcohol. Food related: Pregnant women should eat well. If a pregnant woman does not receive enough folic acid with her food, the child can get neural tube defects.
Sensible precautions
Many women give up cigarettes and alcohol when pregnant, because this gives the embryo a better chance of developing normally.[7]
How common birth defects are
About 3 percent of all babies have what is called a major physical anomaly. This is something that damages the way the baby looks, or how it functions (its physiology).[8]
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. The human brain has had changes and expansion fairly recently in evolutionary terms.
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. 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 (in modern times) 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.[9]
Miscarriages
Spontaneous abortion (miscarriages) have similar causes to birth defects. Many will be due to failures in the genetics controlling development of the embryo.
Most clinically apparent miscarriages (two thirds to three-quarters in various studies) occur during the first trimester.[10][11] Chromosomal abnormalities are found in more than half of embryos miscarried in the first 13 weeks.
A pregnancy with a genetic problem has a 95% probability of ending in miscarriage.[12] Genetic problems are more likely to occur with older parents; this may account for the higher miscarriage rates observed in older women.[13]
Related pages
- List of genetic disorders
- Prenatal diagnostics and amniocentesis
- Apgar score
- Charles II of Spain (pictured at the top of the article)
References
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