Back متلازمة الصبغي X الهش Arabic Martin-Bell sindromu Azerbaijani Síndrome X fràgil Catalan Fragiles-X-Syndrom German Σύνδρομο ευθραύστου χρωμοτοσώματος X Greek Fragile X syndrome English Fragila X sindromo Esperanto Síndrome X frágil Spanish X hauskorraren sindrome Basque سندرم ایکس شکننده Persian
| Fragile X syndrome | |
|---|---|
| Classification and external resources | |
 Location of FMR1 gene | |
| ICD-10 | Q99.2 |
| ICD-9 | 759.83 |
| OMIM | 300624 |
| DiseasesDB | 4973 |
| MedlinePlus | 001668 |
| eMedicine | ped/800 |
| MeSH | D005600 |
Fragile X syndrome (FXS) is a genetic syndrome that causes a range of intellectual disabilities as well as unusual physical and behavioural characteristics. Males and females can have FXS but it is more common, and often more serious, in males.[1] It is one of the most common causes of autism and intellectual disability among boys.[2][3] Individuals with this condition lack an important gene product.[1]
- ↑ 1.0 1.1 CDC (2022-06-03). "What is Fragile X Syndrome (FXS)? | CDC". Centers for Disease Control and Prevention. Retrieved 2023-01-11.
- ↑ Cite error: The named reference
McLennanwas used but no text was provided for refs named (see the help page). - ↑ Budimirovic D.B. & Kaufmann W.E. 2011 (2011). "What can we learn about autism from studying fragile X syndrome?". Dev Neurosci. 33 (5): 379–94. doi:10.1159/000330213. PMC 3254037. PMID 21893949. Retrieved 26 January 2012.
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