.. AMP conducts survey on Genetic Test Registry Today, the Association for Molecular Pathology submitted written feedback in response to the Obtain Information created by the National Institutes of Health for its Genetic Check Registry . AMP executed a survey of its membership to formulate a thorough response to the RFI. With the vast majority of respondents working in a scientific laboratory setting, AMP will be able to inform the NIH on the overall a reaction to the GTR, including insight to the community’s problems and guidance to guarantee the GTR is certainly a valued resource, said Dr. Karen Mann, President of AMP. AMP members reported the next reasons for participating in a voluntary registry: to provide a reference for clinicians and the general public about what tests are offered, to increase transparency of tests, to supply a resource for health care professionals, to streamline screening, to boost data sharing, and to standardize tests.Individuals who do not respond to or aren’t candidates for hydroxyurea treatment can be considered for chronic transfusion therapy. We need to continue our study initiatives into this disease and its management to understand what the optimal treatment routine for these patients is. The majority of our current recommendations are limited by a lack of large-scale clinical trials in this populace. said Dr. Klings. Management of individuals with sickle cell disease with an increased risk for mortality and pulmonary hypertension will eventually be a collaborative effort including adult and pediatric pulmonologists, cardiologists, and hematologists.
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