What is Klinefelter syndrome?
Klinefelter syndrome is a genetic pathology of men, based on endocrine disorders caused by additional female chromosomes in the set of sex chromosomes. This is a fairly common genetic disease.…

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In which ear buzzes: with what is tinnitus connected
In which ear rings? Familiar phrase? The appearance of an unpleasant whistling or monotonous ringing in the auricle can seriously annoy a person and reduce the quality of life. However,…

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In which ear buzzes: with what is tinnitus connected
In which ear rings? Familiar phrase? The appearance of an unpleasant whistling or monotonous ringing in the auricle can seriously annoy a person and reduce the quality of life. However,…

Continue reading →

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

High-risk oncogenic HPV: what is the danger?
Ordinary wart and malignant tumor - what do they have in common? No, no, the wart does not turn into cancer. However, there is something that unites them - is…

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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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