Method, device and system for detecting and analyzing inherited metabolic diseases of newborns
An analysis method and technology of an analysis device, which are applied in the fields of laboratory analysis data, medical informatics, medical automation diagnosis, etc., can solve the problems of not representing the disease of children, the interpretation results are simple and unprofessional, and easy to make mistakes, etc. The effect of traceability and repeated comparison and research in the later period, reducing the investment of labor costs, and high professionalism and authority
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[0027] In order to have a clearer understanding of the technical features, purposes and effects of the present invention, the specific implementation manners of the present invention will now be described with reference to the accompanying drawings.
[0028] Such as figure 1 As shown, a neonatal genetic metabolic disease detection and analysis system includes a data acquisition terminal, a neonatal genetic metabolic disease detection and analysis device; a neonatal genetic metabolic disease detection and analysis device includes a data server, an analysis terminal, and a display terminal; the data acquisition The terminal, the data server, the analysis terminal and the display terminal are sequentially connected, and the data acquisition terminal includes an information entry module and a sample detection module; the data server stores the newborn information database and the disease database; the analysis terminal is used to obtain the information from the data The detection ...
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