A multidisciplinary approach to the management of individuals with fragile X syndrome

Background  Fragile X syndrome (FXS) is the most common inherited form of intellectual disability. Since the identification of the responsible gene (FMR1) and its protein (FMRP), there has been enormous progress in both clinical and pathogenetic research on the neurobehavioural aspects of the condit...

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Veröffentlicht in:Journal of intellectual disability research 2007-02, Vol.51 (2), p.151-161
Hauptverfasser: Alanay, Y., Ünal, F., Turanlı, G., Alikaşifoğlu, M., Alehan, D., Akyol, U., Belgin, E., Şener, C., Aktaş, D., Boduroğlu, K., Utine, E., Volkan-Salancı, B., Özusta, Ş., Genç, A., Başar, F., Sevinç, Ş., Tunçbilek, E.
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container_end_page 161
container_issue 2
container_start_page 151
container_title Journal of intellectual disability research
container_volume 51
creator Alanay, Y.
Ünal, F.
Turanlı, G.
Alikaşifoğlu, M.
Alehan, D.
Akyol, U.
Belgin, E.
Şener, C.
Aktaş, D.
Boduroğlu, K.
Utine, E.
Volkan-Salancı, B.
Özusta, Ş.
Genç, A.
Başar, F.
Sevinç, Ş.
Tunçbilek, E.
description Background  Fragile X syndrome (FXS) is the most common inherited form of intellectual disability. Since the identification of the responsible gene (FMR1) and its protein (FMRP), there has been enormous progress in both clinical and pathogenetic research on the neurobehavioural aspects of the condition. However, studies regarding other medical problems anticipated in individuals with FXS are limited. A multidisciplinary study evaluating various causes of morbidity in the same group has not been published yet. Methods  Twenty‐four boys with FXS full mutation were recruited out of a larger group of 103 diagnosed in one centre over the past 10 years. Ear nose and throat, eye and cardiac examinations were performed in addition to routine cognitive, behavioural, neurological and speech and language assessments. Results  The average IQ score was 49.8 ± 20 (range 25–90). There were four patients (18%) with IQ above 70. Using DSM‐IV, attention deficit hyperactivity disorder was diagnosed in five boys out of 22 examined (23%), while 32% were diagnosed with pervasive developmental disorder. The seizure frequency was 17%. A psychiatric disorder was diagnosed in six out of eight boys with electroencephalogram abnormalities (75%). Minimal conductive hearing loss was found in five (5/22) patients. There was significant delay in both expressive and receptive language skills. Ocular findings were refractive errors (13%) and strabismus (4.4%). Mitral valve prolapsus (MVP) was observed in 3/22 (13.7%) patients and aortic annulus dilatation was present in 2/22 (9%) patients. Conclusions  Frequency of psychiatric diagnoses made with DSM‐IV were in parallel to those reported in the literature. Comorbidity of seizures and psychiatric disorders was noteworthy. The percentage of ‘high‐functioning’ full mutation males supports the previous observations. Ear nose and throat and eye examination revealed remarkably lower prevalence of abnormal findings than reported. MVP was slightly less frequent compared with the single study in the literature. Age at the time of examination had an effect on the outcome of cardiac evaluation. These findings will guide us in future management of the group of patients followed in our institution. The protocol applied provides an applicable outline for multidisciplinary institutional settings dealing with individuals with FXS.
doi_str_mv 10.1111/j.1365-2788.2006.00942.x
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Since the identification of the responsible gene (FMR1) and its protein (FMRP), there has been enormous progress in both clinical and pathogenetic research on the neurobehavioural aspects of the condition. However, studies regarding other medical problems anticipated in individuals with FXS are limited. A multidisciplinary study evaluating various causes of morbidity in the same group has not been published yet. Methods  Twenty‐four boys with FXS full mutation were recruited out of a larger group of 103 diagnosed in one centre over the past 10 years. Ear nose and throat, eye and cardiac examinations were performed in addition to routine cognitive, behavioural, neurological and speech and language assessments. Results  The average IQ score was 49.8 ± 20 (range 25–90). There were four patients (18%) with IQ above 70. Using DSM‐IV, attention deficit hyperactivity disorder was diagnosed in five boys out of 22 examined (23%), while 32% were diagnosed with pervasive developmental disorder. The seizure frequency was 17%. A psychiatric disorder was diagnosed in six out of eight boys with electroencephalogram abnormalities (75%). Minimal conductive hearing loss was found in five (5/22) patients. There was significant delay in both expressive and receptive language skills. Ocular findings were refractive errors (13%) and strabismus (4.4%). Mitral valve prolapsus (MVP) was observed in 3/22 (13.7%) patients and aortic annulus dilatation was present in 2/22 (9%) patients. Conclusions  Frequency of psychiatric diagnoses made with DSM‐IV were in parallel to those reported in the literature. Comorbidity of seizures and psychiatric disorders was noteworthy. The percentage of ‘high‐functioning’ full mutation males supports the previous observations. Ear nose and throat and eye examination revealed remarkably lower prevalence of abnormal findings than reported. MVP was slightly less frequent compared with the single study in the literature. Age at the time of examination had an effect on the outcome of cardiac evaluation. These findings will guide us in future management of the group of patients followed in our institution. The protocol applied provides an applicable outline for multidisciplinary institutional settings dealing with individuals with FXS.</description><identifier>ISSN: 0964-2633</identifier><identifier>EISSN: 1365-2788</identifier><identifier>DOI: 10.1111/j.1365-2788.2006.00942.x</identifier><identifier>PMID: 17217479</identifier><identifier>CODEN: JIDREN</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult and adolescent clinical studies ; Aortic Diseases - diagnosis ; Aortic Diseases - epidemiology ; Attention Deficit Disorder with Hyperactivity - diagnosis ; Attention Deficit Disorder with Hyperactivity - epidemiology ; Attention Deficit Disorders ; Attention Deficit Hyperactivity Disorder ; Biological and medical sciences ; Boys ; Children &amp; youth ; Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...) ; Cognition Disorders - diagnosis ; Cognition Disorders - epidemiology ; Comorbidity ; Developmental Delays ; Diagnostic and Statistical Manual of Mental Disorders ; Ear nose and throat ; fragile X ; Fragile X syndrome ; Fragile X Syndrome - epidemiology ; Fragile X Syndrome - therapy ; Genes ; Genetics ; Hearing Impairments ; Hearing Loss, Conductive - diagnosis ; Hearing Loss, Conductive - epidemiology ; Heart Disorders ; Humans ; Intellectual deficiency ; intellectual disability ; Intelligence Quotient ; Interdisciplinary Approach ; Language Skills ; Learning disabilities ; Male ; Males ; Medical genetics ; Medical sciences ; Medical Services ; Mental Disorders ; Mental Disorders - epidemiology ; Mental Disorders - psychology ; Mental Retardation ; Mitral Valve Prolapse - diagnosis ; Mitral Valve Prolapse - epidemiology ; multidisciplinary approach ; Patient Care - methods ; Patient Care Team ; Patients ; Pervasive Developmental Disorders ; Psychiatric disorders ; Psychiatry ; Psychology. Psychoanalysis. Psychiatry ; Psychopathology. Psychiatry ; Receptive Language ; Refractive Errors - diagnosis ; Refractive Errors - epidemiology ; Seizure ; Seizures ; Seizures - epidemiology ; Strabismus - diagnosis ; Strabismus - epidemiology ; Surveys and Questionnaires ; Visual Impairments</subject><ispartof>Journal of intellectual disability research, 2007-02, Vol.51 (2), p.151-161</ispartof><rights>2007 INIST-CNRS</rights><rights>Copyright Blackwell Publishing Feb 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5142-4b4a459022c38d292a18353c42552773085f8e7a3055947a81e7632bd10bd3fa3</citedby><cites>FETCH-LOGICAL-c5142-4b4a459022c38d292a18353c42552773085f8e7a3055947a81e7632bd10bd3fa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2788.2006.00942.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2788.2006.00942.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,30998,30999,45573,45574</link.rule.ids><backlink>$$Uhttp://eric.ed.gov/ERICWebPortal/detail?accno=EJ749589$$DView record in ERIC$$Hfree_for_read</backlink><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=18486028$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17217479$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alanay, Y.</creatorcontrib><creatorcontrib>Ünal, F.</creatorcontrib><creatorcontrib>Turanlı, G.</creatorcontrib><creatorcontrib>Alikaşifoğlu, M.</creatorcontrib><creatorcontrib>Alehan, D.</creatorcontrib><creatorcontrib>Akyol, U.</creatorcontrib><creatorcontrib>Belgin, E.</creatorcontrib><creatorcontrib>Şener, C.</creatorcontrib><creatorcontrib>Aktaş, D.</creatorcontrib><creatorcontrib>Boduroğlu, K.</creatorcontrib><creatorcontrib>Utine, E.</creatorcontrib><creatorcontrib>Volkan-Salancı, B.</creatorcontrib><creatorcontrib>Özusta, Ş.</creatorcontrib><creatorcontrib>Genç, A.</creatorcontrib><creatorcontrib>Başar, F.</creatorcontrib><creatorcontrib>Sevinç, Ş.</creatorcontrib><creatorcontrib>Tunçbilek, E.</creatorcontrib><title>A multidisciplinary approach to the management of individuals with fragile X syndrome</title><title>Journal of intellectual disability research</title><addtitle>J Intellect Disabil Res</addtitle><description>Background  Fragile X syndrome (FXS) is the most common inherited form of intellectual disability. Since the identification of the responsible gene (FMR1) and its protein (FMRP), there has been enormous progress in both clinical and pathogenetic research on the neurobehavioural aspects of the condition. However, studies regarding other medical problems anticipated in individuals with FXS are limited. A multidisciplinary study evaluating various causes of morbidity in the same group has not been published yet. Methods  Twenty‐four boys with FXS full mutation were recruited out of a larger group of 103 diagnosed in one centre over the past 10 years. Ear nose and throat, eye and cardiac examinations were performed in addition to routine cognitive, behavioural, neurological and speech and language assessments. Results  The average IQ score was 49.8 ± 20 (range 25–90). There were four patients (18%) with IQ above 70. Using DSM‐IV, attention deficit hyperactivity disorder was diagnosed in five boys out of 22 examined (23%), while 32% were diagnosed with pervasive developmental disorder. The seizure frequency was 17%. A psychiatric disorder was diagnosed in six out of eight boys with electroencephalogram abnormalities (75%). Minimal conductive hearing loss was found in five (5/22) patients. There was significant delay in both expressive and receptive language skills. Ocular findings were refractive errors (13%) and strabismus (4.4%). Mitral valve prolapsus (MVP) was observed in 3/22 (13.7%) patients and aortic annulus dilatation was present in 2/22 (9%) patients. Conclusions  Frequency of psychiatric diagnoses made with DSM‐IV were in parallel to those reported in the literature. Comorbidity of seizures and psychiatric disorders was noteworthy. The percentage of ‘high‐functioning’ full mutation males supports the previous observations. Ear nose and throat and eye examination revealed remarkably lower prevalence of abnormal findings than reported. MVP was slightly less frequent compared with the single study in the literature. Age at the time of examination had an effect on the outcome of cardiac evaluation. These findings will guide us in future management of the group of patients followed in our institution. The protocol applied provides an applicable outline for multidisciplinary institutional settings dealing with individuals with FXS.</description><subject>Adult and adolescent clinical studies</subject><subject>Aortic Diseases - diagnosis</subject><subject>Aortic Diseases - epidemiology</subject><subject>Attention Deficit Disorder with Hyperactivity - diagnosis</subject><subject>Attention Deficit Disorder with Hyperactivity - epidemiology</subject><subject>Attention Deficit Disorders</subject><subject>Attention Deficit Hyperactivity Disorder</subject><subject>Biological and medical sciences</subject><subject>Boys</subject><subject>Children &amp; youth</subject><subject>Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)</subject><subject>Cognition Disorders - diagnosis</subject><subject>Cognition Disorders - epidemiology</subject><subject>Comorbidity</subject><subject>Developmental Delays</subject><subject>Diagnostic and Statistical Manual of Mental Disorders</subject><subject>Ear nose and throat</subject><subject>fragile X</subject><subject>Fragile X syndrome</subject><subject>Fragile X Syndrome - epidemiology</subject><subject>Fragile X Syndrome - therapy</subject><subject>Genes</subject><subject>Genetics</subject><subject>Hearing Impairments</subject><subject>Hearing Loss, Conductive - diagnosis</subject><subject>Hearing Loss, Conductive - epidemiology</subject><subject>Heart Disorders</subject><subject>Humans</subject><subject>Intellectual deficiency</subject><subject>intellectual disability</subject><subject>Intelligence Quotient</subject><subject>Interdisciplinary Approach</subject><subject>Language Skills</subject><subject>Learning disabilities</subject><subject>Male</subject><subject>Males</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Medical Services</subject><subject>Mental Disorders</subject><subject>Mental Disorders - epidemiology</subject><subject>Mental Disorders - psychology</subject><subject>Mental Retardation</subject><subject>Mitral Valve Prolapse - diagnosis</subject><subject>Mitral Valve Prolapse - epidemiology</subject><subject>multidisciplinary approach</subject><subject>Patient Care - methods</subject><subject>Patient Care Team</subject><subject>Patients</subject><subject>Pervasive Developmental Disorders</subject><subject>Psychiatric disorders</subject><subject>Psychiatry</subject><subject>Psychology. Psychoanalysis. Psychiatry</subject><subject>Psychopathology. Psychiatry</subject><subject>Receptive Language</subject><subject>Refractive Errors - diagnosis</subject><subject>Refractive Errors - epidemiology</subject><subject>Seizure</subject><subject>Seizures</subject><subject>Seizures - epidemiology</subject><subject>Strabismus - diagnosis</subject><subject>Strabismus - epidemiology</subject><subject>Surveys and Questionnaires</subject><subject>Visual Impairments</subject><issn>0964-2633</issn><issn>1365-2788</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>7QJ</sourceid><recordid>eNqNkV1rFDEYhQdR7Fr9ByJBUK9mTd58gzel1H64aBFLvQvZmUw363ysyYzd_fdmnGULXoi5SeA85_C-OVmGCJ6TdN6v54QKnoNUag4YiznGmsF8-yibHYTH2QxrwXIQlB5lz2Jc40QSJp5mR0QCkUzqWXZzgpqh7n3pY-E3tW9t2CG72YTOFivUd6hfOdTY1t65xrU96irk29L_8uVg64jufb9CVbB3vnboO4q7tgxd455nT6okuxf7-zi7-Xj27fQiX3w5vzw9WeQFJwxytmSWcY0BCqpK0GCJopwWDDgHKSlWvFJOWoo510xaRZwUFJYlwcuSVpYeZ--m3DTvz8HF3jRpD1fXtnXdEI0mWgtNABL59p-kUAwAJE3g67_AdTeENm1hAJQAyvGYpiaoCF2MwVVmE3yTvs4QbMaGzNqMRZixCDM2ZP40ZLbJ-mqfPywbVz4Y95Uk4M0esLGwdfrctvDxgVNMCQwqcS8nzgVfHOSzK8k0V2PMh0m-T9Xs_ns-c3X5NT2SPZ_sPvZue7Db8MMISSU3t5_PzeL60zVd3EpzQX8DcBrCLw</recordid><startdate>200702</startdate><enddate>200702</enddate><creator>Alanay, Y.</creator><creator>Ünal, F.</creator><creator>Turanlı, G.</creator><creator>Alikaşifoğlu, M.</creator><creator>Alehan, D.</creator><creator>Akyol, U.</creator><creator>Belgin, E.</creator><creator>Şener, C.</creator><creator>Aktaş, D.</creator><creator>Boduroğlu, K.</creator><creator>Utine, E.</creator><creator>Volkan-Salancı, B.</creator><creator>Özusta, Ş.</creator><creator>Genç, A.</creator><creator>Başar, F.</creator><creator>Sevinç, Ş.</creator><creator>Tunçbilek, E.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell Publishing</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>7SW</scope><scope>BJH</scope><scope>BNH</scope><scope>BNI</scope><scope>BNJ</scope><scope>BNO</scope><scope>ERI</scope><scope>PET</scope><scope>REK</scope><scope>WWN</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QJ</scope><scope>7X8</scope></search><sort><creationdate>200702</creationdate><title>A multidisciplinary approach to the management of individuals with fragile X syndrome</title><author>Alanay, Y. ; Ünal, F. ; Turanlı, G. ; Alikaşifoğlu, M. ; Alehan, D. ; Akyol, U. ; Belgin, E. ; Şener, C. ; Aktaş, D. ; Boduroğlu, K. ; Utine, E. ; Volkan-Salancı, B. ; Özusta, Ş. ; Genç, A. ; Başar, F. ; Sevinç, Ş. ; Tunçbilek, E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5142-4b4a459022c38d292a18353c42552773085f8e7a3055947a81e7632bd10bd3fa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult and adolescent clinical studies</topic><topic>Aortic Diseases - diagnosis</topic><topic>Aortic Diseases - epidemiology</topic><topic>Attention Deficit Disorder with Hyperactivity - diagnosis</topic><topic>Attention Deficit Disorder with Hyperactivity - epidemiology</topic><topic>Attention Deficit Disorders</topic><topic>Attention Deficit Hyperactivity Disorder</topic><topic>Biological and medical sciences</topic><topic>Boys</topic><topic>Children &amp; youth</topic><topic>Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)</topic><topic>Cognition Disorders - diagnosis</topic><topic>Cognition Disorders - epidemiology</topic><topic>Comorbidity</topic><topic>Developmental Delays</topic><topic>Diagnostic and Statistical Manual of Mental Disorders</topic><topic>Ear nose and throat</topic><topic>fragile X</topic><topic>Fragile X syndrome</topic><topic>Fragile X Syndrome - epidemiology</topic><topic>Fragile X Syndrome - therapy</topic><topic>Genes</topic><topic>Genetics</topic><topic>Hearing Impairments</topic><topic>Hearing Loss, Conductive - diagnosis</topic><topic>Hearing Loss, Conductive - epidemiology</topic><topic>Heart Disorders</topic><topic>Humans</topic><topic>Intellectual deficiency</topic><topic>intellectual disability</topic><topic>Intelligence Quotient</topic><topic>Interdisciplinary Approach</topic><topic>Language Skills</topic><topic>Learning disabilities</topic><topic>Male</topic><topic>Males</topic><topic>Medical genetics</topic><topic>Medical sciences</topic><topic>Medical Services</topic><topic>Mental Disorders</topic><topic>Mental Disorders - epidemiology</topic><topic>Mental Disorders - psychology</topic><topic>Mental Retardation</topic><topic>Mitral Valve Prolapse - diagnosis</topic><topic>Mitral Valve Prolapse - epidemiology</topic><topic>multidisciplinary approach</topic><topic>Patient Care - methods</topic><topic>Patient Care Team</topic><topic>Patients</topic><topic>Pervasive Developmental Disorders</topic><topic>Psychiatric disorders</topic><topic>Psychiatry</topic><topic>Psychology. Psychoanalysis. Psychiatry</topic><topic>Psychopathology. Psychiatry</topic><topic>Receptive Language</topic><topic>Refractive Errors - diagnosis</topic><topic>Refractive Errors - epidemiology</topic><topic>Seizure</topic><topic>Seizures</topic><topic>Seizures - epidemiology</topic><topic>Strabismus - diagnosis</topic><topic>Strabismus - epidemiology</topic><topic>Surveys and Questionnaires</topic><topic>Visual Impairments</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alanay, Y.</creatorcontrib><creatorcontrib>Ünal, F.</creatorcontrib><creatorcontrib>Turanlı, G.</creatorcontrib><creatorcontrib>Alikaşifoğlu, M.</creatorcontrib><creatorcontrib>Alehan, D.</creatorcontrib><creatorcontrib>Akyol, U.</creatorcontrib><creatorcontrib>Belgin, E.</creatorcontrib><creatorcontrib>Şener, C.</creatorcontrib><creatorcontrib>Aktaş, D.</creatorcontrib><creatorcontrib>Boduroğlu, K.</creatorcontrib><creatorcontrib>Utine, E.</creatorcontrib><creatorcontrib>Volkan-Salancı, B.</creatorcontrib><creatorcontrib>Özusta, Ş.</creatorcontrib><creatorcontrib>Genç, A.</creatorcontrib><creatorcontrib>Başar, F.</creatorcontrib><creatorcontrib>Sevinç, Ş.</creatorcontrib><creatorcontrib>Tunçbilek, E.</creatorcontrib><collection>Istex</collection><collection>ERIC</collection><collection>ERIC (Ovid)</collection><collection>ERIC</collection><collection>ERIC</collection><collection>ERIC (Legacy Platform)</collection><collection>ERIC( SilverPlatter )</collection><collection>ERIC</collection><collection>ERIC PlusText (Legacy Platform)</collection><collection>Education Resources Information Center (ERIC)</collection><collection>ERIC</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Applied Social Sciences Index &amp; Abstracts (ASSIA)</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of intellectual disability research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alanay, Y.</au><au>Ünal, F.</au><au>Turanlı, G.</au><au>Alikaşifoğlu, M.</au><au>Alehan, D.</au><au>Akyol, U.</au><au>Belgin, E.</au><au>Şener, C.</au><au>Aktaş, D.</au><au>Boduroğlu, K.</au><au>Utine, E.</au><au>Volkan-Salancı, B.</au><au>Özusta, Ş.</au><au>Genç, A.</au><au>Başar, F.</au><au>Sevinç, Ş.</au><au>Tunçbilek, E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><ericid>EJ749589</ericid><atitle>A multidisciplinary approach to the management of individuals with fragile X syndrome</atitle><jtitle>Journal of intellectual disability research</jtitle><addtitle>J Intellect Disabil Res</addtitle><date>2007-02</date><risdate>2007</risdate><volume>51</volume><issue>2</issue><spage>151</spage><epage>161</epage><pages>151-161</pages><issn>0964-2633</issn><eissn>1365-2788</eissn><coden>JIDREN</coden><abstract>Background  Fragile X syndrome (FXS) is the most common inherited form of intellectual disability. Since the identification of the responsible gene (FMR1) and its protein (FMRP), there has been enormous progress in both clinical and pathogenetic research on the neurobehavioural aspects of the condition. However, studies regarding other medical problems anticipated in individuals with FXS are limited. A multidisciplinary study evaluating various causes of morbidity in the same group has not been published yet. Methods  Twenty‐four boys with FXS full mutation were recruited out of a larger group of 103 diagnosed in one centre over the past 10 years. Ear nose and throat, eye and cardiac examinations were performed in addition to routine cognitive, behavioural, neurological and speech and language assessments. Results  The average IQ score was 49.8 ± 20 (range 25–90). There were four patients (18%) with IQ above 70. Using DSM‐IV, attention deficit hyperactivity disorder was diagnosed in five boys out of 22 examined (23%), while 32% were diagnosed with pervasive developmental disorder. The seizure frequency was 17%. A psychiatric disorder was diagnosed in six out of eight boys with electroencephalogram abnormalities (75%). Minimal conductive hearing loss was found in five (5/22) patients. There was significant delay in both expressive and receptive language skills. Ocular findings were refractive errors (13%) and strabismus (4.4%). Mitral valve prolapsus (MVP) was observed in 3/22 (13.7%) patients and aortic annulus dilatation was present in 2/22 (9%) patients. Conclusions  Frequency of psychiatric diagnoses made with DSM‐IV were in parallel to those reported in the literature. Comorbidity of seizures and psychiatric disorders was noteworthy. The percentage of ‘high‐functioning’ full mutation males supports the previous observations. Ear nose and throat and eye examination revealed remarkably lower prevalence of abnormal findings than reported. MVP was slightly less frequent compared with the single study in the literature. Age at the time of examination had an effect on the outcome of cardiac evaluation. These findings will guide us in future management of the group of patients followed in our institution. The protocol applied provides an applicable outline for multidisciplinary institutional settings dealing with individuals with FXS.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17217479</pmid><doi>10.1111/j.1365-2788.2006.00942.x</doi><tpages>11</tpages></addata></record>
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1365-2788
language eng
recordid cdi_proquest_miscellaneous_919969122
source MEDLINE; Applied Social Sciences Index & Abstracts (ASSIA); EBSCOhost Education Source; Wiley Online Library All Journals
subjects Adult and adolescent clinical studies
Aortic Diseases - diagnosis
Aortic Diseases - epidemiology
Attention Deficit Disorder with Hyperactivity - diagnosis
Attention Deficit Disorder with Hyperactivity - epidemiology
Attention Deficit Disorders
Attention Deficit Hyperactivity Disorder
Biological and medical sciences
Boys
Children & youth
Chromosome fragility (bloom syndrome, ataxia telangiectasia, fanconi anemia, x-linked mental retardation...)
Cognition Disorders - diagnosis
Cognition Disorders - epidemiology
Comorbidity
Developmental Delays
Diagnostic and Statistical Manual of Mental Disorders
Ear nose and throat
fragile X
Fragile X syndrome
Fragile X Syndrome - epidemiology
Fragile X Syndrome - therapy
Genes
Genetics
Hearing Impairments
Hearing Loss, Conductive - diagnosis
Hearing Loss, Conductive - epidemiology
Heart Disorders
Humans
Intellectual deficiency
intellectual disability
Intelligence Quotient
Interdisciplinary Approach
Language Skills
Learning disabilities
Male
Males
Medical genetics
Medical sciences
Medical Services
Mental Disorders
Mental Disorders - epidemiology
Mental Disorders - psychology
Mental Retardation
Mitral Valve Prolapse - diagnosis
Mitral Valve Prolapse - epidemiology
multidisciplinary approach
Patient Care - methods
Patient Care Team
Patients
Pervasive Developmental Disorders
Psychiatric disorders
Psychiatry
Psychology. Psychoanalysis. Psychiatry
Psychopathology. Psychiatry
Receptive Language
Refractive Errors - diagnosis
Refractive Errors - epidemiology
Seizure
Seizures
Seizures - epidemiology
Strabismus - diagnosis
Strabismus - epidemiology
Surveys and Questionnaires
Visual Impairments
title A multidisciplinary approach to the management of individuals with fragile X syndrome
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