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On Feb. 19 the U.S. Food and Drug Administration took a huge step toward patient-centric medicine when it approved the marketing of genetics-testing company 23andMe's carrier test for Bloom syndrome.
"As new technologies come out in health care, it's really important for everyone that there's transparency". The FDA's approval of the marketing of genetics-testing company 23andMe's carrier test for Bloom syndrome affirmed the rights of consumers to drive their own healthcare decisions and procedures.
Their goal: Aid development of a carrier test for the mysterious genetic disorder so breeders could cull their flocks and protect the rare sheep.
Developments in this area continue to emerge and the FDA recently authorized marketing for 23andMe's Bloom Syndrome carrier test, while also planning to exempt future carrier screening tests from premarket review.
This need has been addressed by designing a universal carrier test: a non-invasive, saliva-based assay for more than 100 Mendelian diseases across all major population groups.
They were significantly less upset at time 2 after receiving the results of their carrier test than at time 1.
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The 4-bus multi-carrier test system, shown in Fig. 3, is introduced with some revisions to demonstrate the characteristics of the proposed methodological framework.
GPs felt somewhat more able to actually carry out a HbP-carrier test compared with midwives.
Although ordering a HbP-carrier test is relatively simple, the interpretation of the results is not always straight forward.
GPs scored the intention of offering a HbP-carrier test to their patients on the basis of ethnicity alone, more negative compared with midwives, who scored almost neutral.
The behaviour of interest in this study was offering patients a HbP-carrier test on the basis of their ethnicity, which was explained to participants in the introduction to the questionnaire.
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