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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Causes of lingering cough
Cough is always accompanied by many unpleasant moments. First, it causes pain in the throat, chest. Secondly, a coughing fit can completely disrupt night sleep. And not only the most…

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Immunomodulators and immunostimulants: the truth and myths about magic pills
If they used to say that all diseases are from nerves, now they are blamed for weakened immunity. In order to strengthen it, a large number of various means are…

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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

When honey can be harmful to the body
Honey has long been perceived as a panacea for most, if not all, diseases. It strengthens the immune system, helps fight colds and even strengthens the heart. However, is everything…

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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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