Fragile X syndrome
Fragile X syndrome is a genetic disorder caused by an alteration in the X chromosome (that is, a change in the DNA structure).
FRAGILE X SYNDROME
What is Fragile X syndrome?
Fragile X syndrome is the most common form of inherited mental retardation.
Fragile X syndrome
Definition
Fragile X syndrome is a genetic condition involving changes in part of the X chromosome.
Fragile X syndrome (FXS)
Fragile X syndrome (FXS), also called Martin-Bell syndrome, is the most common type of inherited intellectual disability (formerly called mental retardation).
Fragile X syndrome
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Fragile X syndrome
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Fragile X Syndrome Causes, Symptoms and Treatment and Related Disorders ...
Fragile X syndrome
Alternate Names : Martin-Bell syndrome, Marker X syndrome
Definition ...
Fragile X Syndrome
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Fragile X Syndrome
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Fragile X syndrome
Fragile X syndrome is the second most common specific cause of learning disability after Downs Syndrome. It affects 1 in 1000 males. A milder form affects 1 in 2500 girls who may have normal intelligence.
Fragile X Syndrome
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What is premature ovarian failure (POF)?
What is fragile X syndrome?
Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. Usually, males are more severely affected by this disorder than females.
Fragile X syndrome is a birth defect occurring in about 2 of every 10,000 live births. It is more common in males, occurring in about 1 out of 3,600 and in about 1 of every 4,000-6,000 females.
Fragile X Syndrome
Fragile X Syndrome is the most common inherited cause of mental impairment, and the most common known cause of autism.
Fragile X syndrome
An X-linked recessive disorder that is the leading cause of genetically inherited mental retardation. Because the mutation (in a gene called FMR-1) is X-linked, boys are affected more frequently and more severely.
Fragile X syndrome: One of the most common causes of inherited mental retardation and neuropsychiatric disease in human beings, affects as many as one in 2000 males and one in 4000 females.
Fragile X syndrome (FXS) is a hereditary disorder of the X chromosome. FXS is the most common cause of inherited mental retardation and the most common known cause of autism. FXS affects 1 in 4000 males and 1 in 6000 females.
Causes ...
Fragile X syndrome- the most common inherited form of IDDs caused by a defect in a specific part of the Fragile X Mental Retardation-1 gene that causes the body to produce low amounts or none of a certain protein.
Fragile X Syndrome
Free Standing School of Professional Psychology
Generalized Anxiety Disorder ...
Fragile X syndrome
Definition
Autism is a developmental disorder that appears in the first 3 years of life, and affects the brain's normal development of social and communication skills.
Fragile X syndrome is a condition caused by a fragile area on the X chromosome. This section of the chromosomes...
Galactosemia
Lactose, or milk sugar, is made up of two simple sugars: glucose and galactose. Classic galactosemia is a condition...
Definition Fragile X syndrome is the most common form of inherited mental retardation. Individuals with this condition have developmental delay, variable levels of mental retardation, and behavioral and emotional difficulties.
The National Fragile X Foundation - Fragile X Syndrome - Support Group
The Panic Center - Support Group
The Panic Center - Anxiety Attacks / Phobias / Agoraphobia - Support Group
The Phoenix Society for Burn Survivors, Inc. - Support Group ...
Fragile X syndrome — Fragile X syndrome is the most common cause of intellectual disability (mental retardation) worldwide. People who have fragile X have a defective gene on the X chromosome.
Milder cases of ovarian failure can occur in fragile X syndrome and other rare inherited conditions that cause partial X-chromosome abnormalities.
Cancer treatments (radiation, chemotherapy, or both).
Most tests look at single genes and are used to diagnose rare genetic disorders, such as Fragile X Syndrome and Duchenne Muscular Dystrophy.
Anatomy, Dentists Practice Patterns, Diencephalic Syndrome, Pituitary, Effect, Generation, Embryonal Neoplasm, Equipment, Diagnostic, Female Contraceptive Devices, Forms [Publication Type], Fragile X Syndrome, Gall Bladder Empyemas, ...
Fragile X Syndrome
Fran's Story: Finding Support When You Have COPD
Franceschetti-Zwalen-Klein Syndrome
Francois dyscephaly syndrome
Fraser Syndrome
Fraser-Francois Syndrome
FRDA
Free Sialic Acid Storage Disorders
Freeman Sheldon Syndrome ...
Down syndrome, fragile X syndrome); prenatal problems (e.g., fetal alcohol syndrome, rubella, malnutrition); problems apparent at birth (e.g., low birth weight and prematurity); and problems that occur after birth (e.g.
autism, Asperger syndrome, autism spectrum disorders, behavioral therapy, brain disorder, communication disorders, echolalia, pervasive development disorders, childhood disintegrative disorder, Rett syndrome, Rett disorder, fragile X syndrome, ...
Neurofibromatosis
Tuberous sclerosis
Fragile X syndrome
Phenylketonuria (PKU)
Möbius syndrome
Epilepsy
Herpes encephalitis
Cytomegalovirus
Problems during pregnancy or delivery
Contracting rubella during pregnancy (a risk for the child) ...
Diagnosis - Fragile X syndrome
Diagnosis - X-linked infantile hypogammaglobulinemia
Diagnosis - Pregnancy-induced hypertension
Diagnosis - Pulmonary hypertension
Diagnosis - Renovascular hypertension ...
Autism is linked to certain medical conditions, including fragile X syndrome, untreated phenylketonuria (PKU), tuberous sclerosis, and congenital rubella syndrome. Fetal exposure to toxins, such as hazardous chemicals, may play a role in autism.
Trinucleotide Repeats: Fragile X Syndrome
Detailed information on trinucleotide repeats, including fragile X syndrome
Types of Chromosome Abnormalities ...
These include Turner's syndrome, a condition in which a woman has only one X chromosome instead of the usual two, and fragile X syndrome, a major cause of mental retardation.
Toxins.
Abnormal genes inherited from parents
Errors when genes combine (eg, Down syndrome , Fragile X syndrome )
Nutritional deficiencies
Metabolic conditions (eg, phenylketonuria (PKU), galactosemia , and congenital hypothyroidism ) ...
Genetic abnormalities, including chromosomal abnormalities (eg, congenital thymic aplasia, fragile X syndrome, Turner's syndrome)
Gonadal dysgenesis (incomplete ovarian development, sometimes secondary to genetic disorders)
Irradiation to pelvis ...
The condition is commonly inherited in connection with fragile X syndrome, which is also the second most common genetic cause of mental disabilities.
Obsessive-compulsive disorder
Tourette's syndrome
Fragile X syndrome
Bowel infections
Tuberous sclerosis ...
Translocation Down Syndrome
Translocations
Trinucleotide Repeats: Fragile X Syndrome
Types of Chromosome Abnormalities ...
Fragile X syndrome
Franceschetti-Klein see Treacher Collins syndrome
Freeman Sheldon syndrome
Friedreich's Ataxia
Frontotemporal Dementia see Frontotemporal Lobar Degeneration, including Frontotemporal Dementia ...
Other children at risk include children with Fragile X syndrome and those who have mental retardation. If you feel your child might be exhibiting signs of autism please contact your child's physician.
Fragile X syndrome
Genetic Syndromes
Hearing Loss
Heart conditions, Hereditary
Hereditary Hemorrhagic Telangiectasia
Inborn Errors of Metabolism
Inherited Skin Disorders
Kidney Disease, Inherited
Long QT Syndrome
Lysosomal Storage Disorders ...
Some people who have autism may also have other disorders that affect the brain. These include:
epilepsy
Down syndrome
fragile X syndrome
Turner syndrome ...
Autism has been associated with some genetic abnormalities, especially on chromosome 15, and it is also found associated with the "fragile X syndrome.
large, a device called an orchidometer is used that permits the testes to be compared to a series of plastic ovals (like miniature American footballs) of differing sizes. Macroorchidism is a diagnostic feature, for example, of the fragile X syndrome, ...
Children with ASDs also are prone to developing separate, co-occurring behavioral or psychiatric problems - epilepsy, Fragile X syndrome, attention deficit disorder, learning disabilities, or Tourette syndrome - that also may require treatment.
Examples of overgrowth syndromes include neurofibromatosis, Sotos syndrome, Beckwith-Wiedemann syndrome, Simpson-Golabi-Behmel syndrome, Weaver syndrome, Proteus syndrome, Sturge-Weber syndrome and fragile X syndrome.
fragile X syndrome
Fraley syndrome
Franceschetti-Jadassohn syndrome
Franceschetti's syndrome
Fraser's syndrome
Freeman-Sheldon syndrome
Frenkel's anterior ocular traumatic syndrome
Frey's syndrome
Friderichsen-Waterhouse syndrome ...
Members of your family have had other inherited problems, such as hemophilia, cystic fibrosis, or fragile X syndrome.
Someone in your family has had sickle cell anemia. This problem causes abnormal red blood cells.
Shapiro's interests involve the delineation and understanding of congenital malformations, mental retardation, cytogenetics and prenatal diagnosis. His most recent research interests have dealt with the Fragile X syndrome.
 See also: Symptom, Mental retardation, Pregnancy, Prevention, Anxiety
  
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