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  1. 15 de may. de 2024 · What is fragile X syndrome (FXS)? Fragile X syndrome (FXS) is a genetic disorder caused by changes in a gene called fragile X messenger ribonucleoprotein 1 (FMR1). FMR1 usually makes a protein called FMRP that is needed for brain development. People who have FXS do not make this protein.

  2. Hace 14 horas · Un caso de síndrome X Frágil y su intervención desde la Atención Infantil Temprana. Electronic Journal of Research in Educational Psychology, 9(3), 1333-1352. Salcedo-Arellano, M. J., Hagerman, R. J. y Martínez-Cerdeño, V. (2020). Fragile X syndrome: clinical presentation, pathology and treatment.

  3. 21 de may. de 2024 · Learn about Fragile X syndrome, a genetic condition that causes intellectual disability, behavioral and learning challenges, and physical characteristics. Find events, resources, research, and support for the Fragile X community.

  4. 15 de may. de 2024 · Fragile X syndrome is a genetic disorder caused by changes in a gene called FMR1. Fact #1: Children are not usually tested for FXS when women are pregnant with them, or right after they are born. FXS requires a special blood test that is not usually included in the genetic tests that a pregnant woman gets or in the tests done right ...

  5. 15 de may. de 2024 · Fragile X syndrome (FXS) is the most common known cause of inherited intellectual disability. 1 FXS affects both males and females, although females often have milder symptoms than males. 2 The exact number of people who have FXS is unknown, but a review of research studies estimated that about 1 in 7,000 males and about 1 in 11,000 ...

  6. Hace 2 días · FRAXA is a nonprofit organization that supports research and clinical trials for Fragile X syndrome, the most common inherited cause of autism and intellectual disabilities. Learn about Fragile X, how to donate, and the latest news and updates from FRAXA.

  7. 25 de may. de 2024 · Fragile X syndrome (FXS) is a genetic disorder caused by a mutation in the fragile X messenger ribonucleoprotein 1 ( FMR1) gene and known to be a leading cause of inherited intellectual disability globally. It results in a range of intellectual, developmental, and behavioral problems.