Hereditary diseases
Hereditary diseases are diseases caused by chromosomal and gene mutations. Some confuse hereditary diseases with congenital diseases. Indeed, congenital diseases, that is, diseases with which a child is born, may…

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Causes of hormonal failure in men and women
About 75% of the adult population suffer from various hormonal disorders. The psychoemotional and physical state of a person directly depends on the synthesis of hormones, with the slightest failure…

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Grandmother's methods: why do I need an iodine net?
Older people remember that in childhood, with bruises or colds, mothers painted a grid with iodine on their bodies. And today, many have not refused such treatment. And what helps…

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occurrence in children

Identify the pathology of the fetus has become easier. DOT test

The birth of a child is a great happiness in the life of a family. And of course, every mother first of all wants her child to be born healthy. Here, of course, planning of pregnancy, lifestyle, proper nutrition of a pregnant woman are very important. But, unfortunately, this is not enough. The health of the unborn child depends on genetic factors. Today, doctors have the opportunity to identify chromosomal abnormalities in the fetus in the very early stages of pregnancy. Continue reading

Reasons to seek advice from genetics

What does a geneticist do?
Medical genetics is a part of human genetics that studies diseases and pathologies caused by heredity. A geneticist studies hereditary diseases and the conditions under which hereditary predisposition is realized. It does not cure any organ or system of the body, it is within its competence to identify the disease associated with genetics, or the risk of its occurrence. Continue reading

8 reasons for early gray hair
Over the years, with us, someone earlier, others later, the hair begins to turn gray. This is quite normal, although it does not please us. But sometimes gray strands are…

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Unusual Diseases: Aarskog Syndrome
Aarskog syndrome, also known as Aaskorg – Scott syndrome, or faciesigiogenital dysplasia, is a very rare hereditary disease: it occurs in one person in a million. It manifests itself with…

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