Massive study screens 100,000 babies for hidden rare diseases
NCT ID NCT05368038
Summary
This study aims to gather information by offering expanded newborn screening to 100,000 babies in New York. It will test for 14 rare genetic disorders to see how accurate the tests are, how often these diseases occur, and if finding them early helps children's health. The main goal is to collect data to help decide if these tests should be offered to all newborns nationwide.
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Contacts and locations
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Locations
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Jack D. Weiler Hospital
The Bronx, New York, 10461, United States
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Long Island Jewish Medical Center
Queens, New York, 11040, United States
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Maimonides Medical Center
Brooklyn, New York, 11219, United States
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Mount Sinai Hospital
New York, New York, 10028, United States
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Mount Sinai West
New York, New York, 10019, United States
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NYU Langone Health - Tisch Hospital
New York, New York, 10016, United States
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NYU Langone Hospital - Brooklyn
Brooklyn, New York, 11220, United States
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North Shore University Hospital
Manhasset, New York, 11030, United States
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ScreenPlus Coordinating Core, Children's Hospital at Montefiore
The Bronx, New York, 10467, United States
Conditions
Explore the condition pages connected to this study.