Fragile X syndrome: Difference between revisions
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== [[Fragile X syndrome overview|Overview]] == | == [[Fragile X syndrome overview|Overview]] == | ||
Fragile x syndrome is the leading inherited cause of intellectual disorder and autism spectrum disorder with severe behavioural alterations . It is an X linked disorder, affecting both males and females. | |||
== [[Fragile X syndrome historical perspective|Historical Perspective]] == | == [[Fragile X syndrome historical perspective|Historical Perspective]] == | ||
Revision as of 11:43, 11 July 2021
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| Fragile X syndrome | |
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| Location of FMR1 gene | |
| ICD-10 | Q99.2 |
| ICD-9 | 759.83 |
| OMIM | 309550 |
| DiseasesDB | 4973 |
| MeSH | D005600 |
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Fragile X syndrome Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Fragile X syndrome On the Web |
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American Roentgen Ray Society Images of Fragile X syndrome |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords:: Martin-bell syndrome; marker X syndrome, escalante's syndrome
Overview
Fragile x syndrome is the leading inherited cause of intellectual disorder and autism spectrum disorder with severe behavioural alterations . It is an X linked disorder, affecting both males and females.
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Fragile X syndrome from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms | Physical Examination | Laboratory Findings | Other Diagnostic Studies
Treatment
Medical Therapy | Primary Prevention | Secondary Prevention | Cost Effectiveness of Therapy | Future or Investigational Therapies
Case Studies
External links
Template:Pervasive developmental disorders Template:Chromosomal abnormalities