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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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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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 & 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>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18486028$$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 & 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 & 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 & 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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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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T17%3A48%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20multidisciplinary%20approach%20to%20the%20management%20of%20individuals%20with%20fragile%20X%20syndrome&rft.jtitle=Journal%20of%20intellectual%20disability%20research&rft.au=Alanay,%20Y.&rft.date=2007-02&rft.volume=51&rft.issue=2&rft.spage=151&rft.epage=161&rft.pages=151-161&rft.issn=0964-2633&rft.eissn=1365-2788&rft.coden=JIDREN&rft_id=info:doi/10.1111/j.1365-2788.2006.00942.x&rft_dat=%3Cproquest_cross%3E68422273%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=228623502&rft_id=info:pmid/17217479&rft_ericid=EJ749589&rfr_iscdi=true |