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Genetic Disorders Write for Us

genetic disorders write for us

Introduction to Genetic Disorders

Genetic disorders are disorders produced by abnormalities in one or more genes or chromosomes. Some genetic disorders are inherited, and others are spontaneous.

  • Hereditary genetic disorders are passed down from generation to generation.
  • Spontaneous genetic disorders are not passed from one generation to another. Still, they occur when the genetic material in the father’s sperm or mother’s eggs or cells of the developing embryo is damaged by chance or by drugs, chemicals, or other harmful substances (such as X-rays).
  • Before becoming pregnant, women and their partners should consult their doctor about the risk of having a child with a genetic disorder.
  • Risk factors include an elderly woman (“old”), family history of genetic abnormalities, spontaneous abortions, a previous child with congenital malformations, and chromosomal abnormalities in one of the future parents.
  • Tests for genetic diseases can remain done in all couples, especially those at a higher than average risk of having babies.



Couples considering having a child should consult about the risk of their future baby suffering from genetic alterations (prenatal genetic counseling). They can discuss the precautions they can take to help avoid some congenital abnormalities. For example, women can prevent contact with toxic substances and energy.

Couples can also request their doctor to determine if the risk of having a baby with genetic alterations in their case is higher than average. If the risk is high, tests will be done to help evaluate it more accurately ( genetic screening ). Therefore, if the result of these tests confirms that there is a high probability of severe genetic alterations.

If the woman is already pregnant, the doctor will inform her of the different tests that can be performed to examine the fetus during pregnancy ( prenatal diagnostic tests). It will also notify you of the possible options if a genetic alteration is detected in these tests. Abortion is one of these options. In some cases, the abnormality can remain treated. Sometimes the couple refer to the consultation of a geneticist, who will help them make the most appropriate decision. Doctors can advise a woman to obtain prenatal care at a center that offers more comprehensive services for newborns.

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