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fragile X syndrome

[fraj-uhl eks sin-drohm, -druhm, frajahyl]

noun

  1. an inherited genetic disorder caused by a faulty gene on the X chromosome and having various possible effects, including developmental delays in infancy and early childhood, learning disabilities, intellectual disability, and a number of social, behavioral, and physical difficulties.



fragile-X syndrome

noun

  1. an inherited condition characterized by mental subnormality: affected individuals have an X-chromosome that is easily damaged under certain conditions

“Collins English Dictionary — Complete & Unabridged” 2012 Digital Edition © William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins Publishers 1998, 2000, 2003, 2005, 2006, 2007, 2009, 2012
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Word History and Origins

Origin of fragile X syndrome1

First recorded in 1980–85
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Example Sentences

Examples are provided to illustrate real-world usage of words in context. Any opinions expressed do not reflect the views of Dictionary.com.

The findings may also have implications for intellectual disabilities, such as Fragile X syndrome.

He has Fragile X syndrome resulting in a learning disability which can impact communication, but not his love for music.

From BBC

Fragile X syndrome, the most common form of inherited intellectual disability, may be unfolding in brain cells even before birth, despite typically going undiagnosed until age 3 or later.

A new study published today in the journal Neuron by researchers at the University of Wisconsin-Madison showed that FMRP, a protein deficient in individuals with fragile X syndrome, has a role in the function of mitochondria, part of a cell that produces energy, during prenatal development.

Their results fundamentally change how scientists understand the developmental origins of fragile X syndrome and suggest a potential treatment for brain cells damaged by the dysfunction.

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