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1. www.fragilex.org.uk › syndromeAbout Fragile X Syndrome | Fragile X Society | UK

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   Fragile X Syndrome (FXS) is a genetic condition, affecting around 1 in 4000 males and 1 in 6000 females. It can cause a wide range of difficulties with learning, as well as social, language, attentional, emotional, and behavioural problems.

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     Fragile X Syndrome - causes, symptoms, diagnosis, treatment, pathology

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     Trisomy 21, Fragile X, Duchenne's Muscular Dystrophy - Pediatrics - Nervous System | @LevelUpRN

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     Introduction to Fragile X Syndrome

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3. www.cdc.gov › fragile-x-syndrome › aboutAbout Fragile X Syndrome | Fragile X Syndrome (FXS) | CDC

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   May 15, 2024 · Fragile X syndrome (FXS) is a genetic disorder and one of the most common causes of inherited intellectual disability. FXS affects both males and females. However, females often have milder symptoms than males.

4. my.clevelandclinic.org › health › diseasesFragile X Syndrome (FXS): What It Is, Symptoms & Treatment

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   Feb 7, 2024 · Fragile X syndrome (FXS) is an inherited genetic disorder that causes physical abnormalities, behavioral issues and a wide range of other health problems. What are the symptoms of fragile X syndrome? Fragile X syndrome affects your child’s intelligence, mental health, physical features and behavior.

5. www.genomicseducation.hee.nhs.uk › genotesFragile X syndrome — Knowledge Hub - GeNotes

   www.genomicseducation.hee.nhs.uk › genotes

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   Fragile X syndrome is an X-linked genetic condition that results in intellectual disability and characteristic dysmorphic features. It usually presents in early childhood and is the most common inherited cause of intellectual disability in boys.

6. en.wikipedia.org › wiki › Fragile_X_syndromeFragile X syndrome - Wikipedia

   en.wikipedia.org › wiki › Fragile_X_syndrome

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   Fragile X syndrome is a genetic disorder which occurs as a result of a mutation of the Fragile X Messenger Ribonucleoprotein 1 (FMR1) gene on the X chromosome, most commonly an increase in the number of CGG trinucleotide repeats in the 5' untranslated region of FMR1.

7. www.nichd.nih.gov › health › topicsFragile X Syndrome - NICHD - Eunice Kennedy Shriver National ...

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   Fragile X syndrome is the most common form of inherited intellectual and developmental disability (IDD). People with Fragile X syndrome may not have noticeable symptoms, or they can have more serious symptoms that range from learning disabilities to cognitive and behavior problems.

8. People also ask

   What is fragile X syndrome?

   • Fragile X syndrome is the most common form of inherited intellectual and developmental disability (IDD). It gets its name because when you look at the X chromosome through a microscope, part of it looks “broken” or “fragile.” Another name for the condition is Martin-Bell syndrome. How common is fragile X syndrome?

   Fragile X Syndrome (FXS): What It Is, Symptoms & Treatment

   my.clevelandclinic.org/health/diseases/5476-fragile-x-syndrome

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   Can a mutation cause fragile X syndrome?

   • People with a full mutation often have Fragile X syndrome. The number of repeats, also called the “size of the mutation,” affects the type of symptoms and how serious the symptoms of Fragile X syndrome will be. Fragile X syndrome is inherited, which means it is passed down from parents to children.

   Fragile X Syndrome - NICHD - Eunice Kennedy Shriver National Institute

   www.nichd.nih.gov/health/topics/factsheets/fragilex

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   Can fragile X syndrome be cured?

   • Fragile X syndrome is a lifelong condition. There’s no cure. What is the life expectancy of fragile X syndrome? None of the symptoms of fragile X syndrome are life-threatening. The fragile X syndrome life expectancy is the same as for the average person. What is life like with fragile X syndrome? Fragile X syndrome affects every child differently.

   Fragile X Syndrome (FXS): What It Is, Symptoms & Treatment

   my.clevelandclinic.org/health/diseases/5476-fragile-x-syndrome

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   What are the symptoms of Fragile X syndrome (FXS)?

   • Fragile X syndrome tends to show more symptoms on affected males since females have another X chromosome which can compensate for the damaged one. Prominent characteristics of the syndrome include an elongated face and large or protruding ears. Most young children do not show any physical signs of FXS.

   Fragile X syndrome - Wikipedia

   en.wikipedia.org/wiki/Fragile_X_syndrome

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   What if my child has Fragile X syndrome?

   • If your child has fragile X syndrome, you should tell your healthcare provider. As a possible carrier, you’re at a higher risk for: Menopause that starts before age 40. Dementia. High blood pressure. Depression. Anxiety. Migraines. Hypothyroidism. Chronic pain. Sleep apnea. What are the complications of fragile X syndrome?

   Fragile X Syndrome (FXS): What It Is, Symptoms & Treatment

   my.clevelandclinic.org/health/diseases/5476-fragile-x-syndrome

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   How many people have fragile X syndrome?

   • 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 females have been diagnosed with FXS. 1 Keep Reading: How Fragile X Syndrome Is Inherited

   About Fragile X Syndrome | Fragile X Syndrome (FXS) | CDC

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9. www.cdc.gov › fragile-x-syndrome › aboutHow Fragile X Syndrome Is Inherited | Fragile X Syndrome (FXS ...

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   At a glance. Fragile X syndrome (FXS) is a genetic disorder. A genetic disorder means that there are changes to the person's genes. FXS, or the risk for developing FXS, can be passed down from parents to children through genes. Here is some information to help you understand how FXS and some related conditions can be passed down through genes.