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A rare genetic disorder, often misdiagnosed, is more common than believed, prompting calls for wider screening.
A new study reveals that a rare genetic condition, previously misdiagnosed in many patients, may be more common than thought, prompting experts to recommend broader genetic screening.
Researchers at the National Institutes of Health identified the disorder in over 200 individuals across diverse populations, with symptoms often mistaken for more common neurological conditions.
Early detection through targeted testing could improve outcomes, according to the findings published in the New England Journal of Medicine.
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Un raro trastorno genético, a menudo diagnosticado erróneamente, es más común de lo que se creía, lo que ha provocado que se soliciten exámenes de detección más amplios.