The Arthropathy of Down Syndrome: An Underdiagnosed and Under-recognized Condition

Objective To define the clinical manifestations, determine prevalence, and heighten awareness about the arthropathy of Down syndrome. Study design Using diagnostic codes for Down syndrome and juvenile idiopathic arthritis (JIA), we identified 9 cases in our hospital system. Each case met diagnostic...

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Veröffentlicht in:The Journal of pediatrics 2009-02, Vol.154 (2), p.234-238
Hauptverfasser: Juj, Harbir, MD, MPH, Emery, Helen, MBBS
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Emery, Helen, MBBS
description Objective To define the clinical manifestations, determine prevalence, and heighten awareness about the arthropathy of Down syndrome. Study design Using diagnostic codes for Down syndrome and juvenile idiopathic arthritis (JIA), we identified 9 cases in our hospital system. Each case met diagnostic criteria for JIA. Cases were compared with 21 additional literature cases. Prevalence was determined with diagnostic codes. Results Average delay from symptom onset to diagnosis was 2 years. Age at onset varied from 20 months to 12 years. Sex distribution was equal. At symptom onset, 57% had polyarticular disease, and 43% had oligoarticular disease, but 54% with oligoarticular disease progressed to polyarticular disease. Seventy-two percent had an elevated erythrocyte sedimentation rate. Most required second-line therapy, and almost half had development of joint subluxation. Prevalence of Down syndrome arthropathy is 8.7/1000, more than 6 times higher than JIA in the general population. Conclusion The arthropathy of Down syndrome is an underrecognized condition that results in chronic disability and functional impairment in a population already at significant risk. Children with Down syndrome are predisposed to autoimmune disorders, but arthritis is overlooked in surveillance guidelines. To maximize joint function and quality of life, providers caring for children with Down syndrome need a high index of suspicion for the related arthropathy.
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Study design Using diagnostic codes for Down syndrome and juvenile idiopathic arthritis (JIA), we identified 9 cases in our hospital system. Each case met diagnostic criteria for JIA. Cases were compared with 21 additional literature cases. Prevalence was determined with diagnostic codes. Results Average delay from symptom onset to diagnosis was 2 years. Age at onset varied from 20 months to 12 years. Sex distribution was equal. At symptom onset, 57% had polyarticular disease, and 43% had oligoarticular disease, but 54% with oligoarticular disease progressed to polyarticular disease. Seventy-two percent had an elevated erythrocyte sedimentation rate. Most required second-line therapy, and almost half had development of joint subluxation. Prevalence of Down syndrome arthropathy is 8.7/1000, more than 6 times higher than JIA in the general population. Conclusion The arthropathy of Down syndrome is an underrecognized condition that results in chronic disability and functional impairment in a population already at significant risk. Children with Down syndrome are predisposed to autoimmune disorders, but arthritis is overlooked in surveillance guidelines. To maximize joint function and quality of life, providers caring for children with Down syndrome need a high index of suspicion for the related arthropathy.</description><identifier>ISSN: 0022-3476</identifier><identifier>EISSN: 1097-6833</identifier><identifier>DOI: 10.1016/j.jpeds.2008.07.056</identifier><identifier>PMID: 18783795</identifier><identifier>CODEN: JOPDAB</identifier><language>eng</language><publisher>Maryland Heights, MO: Mosby, Inc</publisher><subject>Adolescent ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Antibodies, Antinuclear - blood ; Antirheumatic Agents - therapeutic use ; Arthritis, Juvenile - complications ; Arthritis, Juvenile - therapy ; Biological and medical sciences ; Child ; Child, Preschool ; Chromosome aberrations ; Contracture - complications ; Disease Progression ; Diseases of the osteoarticular system ; Down Syndrome - complications ; Female ; General aspects ; Humans ; Infant ; Joint Dislocations - complications ; Male ; Medical genetics ; Medical sciences ; Miscellaneous. 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Study design Using diagnostic codes for Down syndrome and juvenile idiopathic arthritis (JIA), we identified 9 cases in our hospital system. Each case met diagnostic criteria for JIA. Cases were compared with 21 additional literature cases. Prevalence was determined with diagnostic codes. Results Average delay from symptom onset to diagnosis was 2 years. Age at onset varied from 20 months to 12 years. Sex distribution was equal. At symptom onset, 57% had polyarticular disease, and 43% had oligoarticular disease, but 54% with oligoarticular disease progressed to polyarticular disease. Seventy-two percent had an elevated erythrocyte sedimentation rate. Most required second-line therapy, and almost half had development of joint subluxation. Prevalence of Down syndrome arthropathy is 8.7/1000, more than 6 times higher than JIA in the general population. Conclusion The arthropathy of Down syndrome is an underrecognized condition that results in chronic disability and functional impairment in a population already at significant risk. Children with Down syndrome are predisposed to autoimmune disorders, but arthritis is overlooked in surveillance guidelines. To maximize joint function and quality of life, providers caring for children with Down syndrome need a high index of suspicion for the related arthropathy.</description><subject>Adolescent</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Antibodies, Antinuclear - blood</subject><subject>Antirheumatic Agents - therapeutic use</subject><subject>Arthritis, Juvenile - complications</subject><subject>Arthritis, Juvenile - therapy</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Chromosome aberrations</subject><subject>Contracture - complications</subject><subject>Disease Progression</subject><subject>Diseases of the osteoarticular system</subject><subject>Down Syndrome - complications</subject><subject>Female</subject><subject>General aspects</subject><subject>Humans</subject><subject>Infant</subject><subject>Joint Dislocations - complications</subject><subject>Male</subject><subject>Medical genetics</subject><subject>Medical sciences</subject><subject>Miscellaneous. 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Osteoarticular involvement in other diseases</topic><topic>Pediatrics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Juj, Harbir, MD, MPH</creatorcontrib><creatorcontrib>Emery, Helen, MBBS</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>The Journal of pediatrics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Juj, Harbir, MD, MPH</au><au>Emery, Helen, MBBS</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Arthropathy of Down Syndrome: An Underdiagnosed and Under-recognized Condition</atitle><jtitle>The Journal of pediatrics</jtitle><addtitle>J Pediatr</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>154</volume><issue>2</issue><spage>234</spage><epage>238</epage><pages>234-238</pages><issn>0022-3476</issn><eissn>1097-6833</eissn><coden>JOPDAB</coden><abstract>Objective To define the clinical manifestations, determine prevalence, and heighten awareness about the arthropathy of Down syndrome. Study design Using diagnostic codes for Down syndrome and juvenile idiopathic arthritis (JIA), we identified 9 cases in our hospital system. Each case met diagnostic criteria for JIA. Cases were compared with 21 additional literature cases. Prevalence was determined with diagnostic codes. Results Average delay from symptom onset to diagnosis was 2 years. Age at onset varied from 20 months to 12 years. Sex distribution was equal. At symptom onset, 57% had polyarticular disease, and 43% had oligoarticular disease, but 54% with oligoarticular disease progressed to polyarticular disease. Seventy-two percent had an elevated erythrocyte sedimentation rate. Most required second-line therapy, and almost half had development of joint subluxation. Prevalence of Down syndrome arthropathy is 8.7/1000, more than 6 times higher than JIA in the general population. Conclusion The arthropathy of Down syndrome is an underrecognized condition that results in chronic disability and functional impairment in a population already at significant risk. Children with Down syndrome are predisposed to autoimmune disorders, but arthritis is overlooked in surveillance guidelines. To maximize joint function and quality of life, providers caring for children with Down syndrome need a high index of suspicion for the related arthropathy.</abstract><cop>Maryland Heights, MO</cop><pub>Mosby, Inc</pub><pmid>18783795</pmid><doi>10.1016/j.jpeds.2008.07.056</doi><tpages>5</tpages></addata></record>
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subjects Adolescent
Anti-Inflammatory Agents, Non-Steroidal - therapeutic use
Antibodies, Antinuclear - blood
Antirheumatic Agents - therapeutic use
Arthritis, Juvenile - complications
Arthritis, Juvenile - therapy
Biological and medical sciences
Child
Child, Preschool
Chromosome aberrations
Contracture - complications
Disease Progression
Diseases of the osteoarticular system
Down Syndrome - complications
Female
General aspects
Humans
Infant
Joint Dislocations - complications
Male
Medical genetics
Medical sciences
Miscellaneous. Osteoarticular involvement in other diseases
Pediatrics
title The Arthropathy of Down Syndrome: An Underdiagnosed and Under-recognized Condition
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