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Conditions
Genetic disease
Chromosomal disorders
Fragile X syndrome

Fragile X syndrome

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A genetic disorder caused by a mutation of the FMR1 gene. Affected individuals may have large heads and long faces.

Dr. Geoffreysss Rutledgeee reviewed this

41 years experience

Is a type of:

Developmental disorders • Chromosomal disorders

How long it usually lasts:

Chronic (lasts years to lifelong)

How common it is:

Rare
Baby
0-2
Very common
Toddler
3-5
Very common
Preteen
6-13
Very common
Teenager
14-18
Very common
Young adult
19-40
Very common
Middle-aged adult
41-60
Senior
60+

How it can usually be treated?

Incurable but treatment can help

How is it usually diagnosed?

Requires diagnosis by a medical professional

Symptoms

Feeling anxious
Hyperactivity
Impulsive or reckless behavior
Speech difficulty
Loss of speech
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Related questions

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What is fragile x syndrome?

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Please tell me, are people with fragile x syndrome tall?

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My son was recently tested for fragile x syndrome. What is accuracy?

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I was wondering what are the social ramifications for those afflicted with fragile x syndrome?

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Is fragile x syndrome dominant or recessive?

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What's the life expectancy of a person with fragile x syndrome?

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Is fragile x syndrome the same degree of retardation as down syndrome?

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Is there a protein affected in fragile x syndrome?

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Do natural remedies for fragile x syndrome work?

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