[Stable osteosynthesis in traumatology and orthopedics].
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Biomedical subjects
Publications and source records attributed to S A Spasov.
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Described is a case with the Mayer-Rokitansky-Küster-Hauser syndrome with normal pubescent female development, moderate hair virilismus, double rudimentary uterus, incomplete development of the vagina, ovarian dystrophy and abnormalities in the sex chromatin and the gonosomal complement. Discussion on the clinical variety and the ethiopathogenesis of the disease is performed.
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Twelve patients with Meyer-Rokitansky-Küster-Hauser syndrome were examined by means of pneumogynecography. The results obtained disclose the great diagnostic value of the method in this disorder.
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Sex chromatin frequency was investigated in nuclei from epithelial cells of the oral mucosa in 20 healthy, mature newborn females in the first 10 days of the neonatal period and compared with the hormonal state of the infant. From the analysis of the results obtained it was evident that sex chromatin incidence of the newborn female fluctuated in the neonatal period in values similar to those of healthy, nonpregnant woman. However, a specific correlation was disclosed between the alterations of the sex chromatin frequency and the hormonal crisis of the newborn infant.
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