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Program search — Hemophilia
Name Hemophilia
Description Bleeding in which the blood does not thicken.
Hemophilia is a classic hereditary disease. Hemophilia affects males. The transmission of the disease occurs through women who are carriers of the symptom. Thus, from the grandfather, the disease is transmitted to the grandson through the mother. The nature of inheritance in hemophilia is associated with changes in unpaired chromosomes and occurs in a recessive manner linked to the X chromosome. In the sexual X chromosome there are genes that determine the synthesis of AHH. If under the influence of any mutagenic effects in children the X chromosome changes and does not carry the gene that determines the synthesis of AHH (such a chromosome is denoted by X "), hemophilia can occur. In women, hemophilia, as a rule, does not occur, since the sex chromosomes of women are represented by two X chromosomes (XX)
Chapter Blood, immune mechanism
ICD-10 class D50-D89
Author Dr. R.Rife
Frequencies, Hz 603
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Blood, immune mechanismBioresonance therapy. Frequencies, Hz: 603