{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,14]],"date-time":"2026-11-14T02:27:52Z","timestamp":1794623272390,"version":"4.9.1"},"reference-count":22,"publisher":"Journal of Neurosurgery Publishing Group (JNSPG)","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2021,8]]},"abstract":"<jats:sec>\n                    <jats:title>OBJECTIVE<\/jats:title>\n                    <jats:p>The authors sought to determine the overall incidence of cervicomedullary decompression (CMD) in patients with achondroplasia and the characteristics associated with those surgeries across multiple institutions with experience caring for individuals with skeletal dysplasias.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>METHODS<\/jats:title>\n                    <jats:p>Data from CLARITY (Achondroplasia Natural History Study) for 1374 patients with achondroplasia from four skeletal dysplasia centers (A. I. duPont Hospital for Children, Johns Hopkins University, University of Texas Health, and University of Wisconsin School of Medicine and Public Health) followed from 1957 to 2017 were recorded in a Research Electronic Data Capture (REDCap) database. Data collected and analyzed included surgeries, indications, complications, ages at time of procedures, screening procedures, and medical diagnoses.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>RESULTS<\/jats:title>\n                    <jats:p>There were 314 CMD procedures in 281 patients (20.5% of the entire cohort). The median age of first CMD was 1.3 years in males and 1.1 years in females. Over time, there was a decrease in the median age of patients at first CMD. All patients born before 1980 who underwent CMD had the procedure after 5 years of age, whereas 98% of patients born after 2010 underwent CMD before 5 years of age. In addition, a greater proportion of patients born in more recent decades had documented neuroimaging and polysomnography (PSG) prior to CMD. Ventriculoperitoneal shunts (VPSs) were placed more frequently in patients undergoing CMD (23%) than in the entire cohort (8%). Patients who required either CMD or VPS were 7 times more likely to require both surgeries than patients who required neither surgery (OR 7.0, 95% CI 4.66\u201310.53; p &lt; 0.0001). Overall, 10.3% of patients who underwent CMD required a subsequent CMD.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>CONCLUSIONS<\/jats:title>\n                    <jats:p>The prevalence of CMD in this large achondroplasia cohort was 20%, with more recently treated patients undergoing first CMD at younger ages than earlier patients. The use of neuroimaging and PSG screening modalities increased over time, suggesting that increased and better surveillance contributed to earlier identification and intervention in patients with cervicomedullary stenosis and its complications.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.3171\/2020.12.peds20715","type":"journal-article","created":{"date-parts":[[2021,6,4]],"date-time":"2021-06-04T03:11:16Z","timestamp":1622776276000},"page":"229-235","source":"Crossref","is-referenced-by-count":17,"title":["Achondroplasia Natural History Study (CLARITY): 60-year experience in cervicomedullary decompression in achondroplasia from four skeletal dysplasia centers"],"prefix":"10.3171","volume":"28","author":[{"given":"Janet M.","family":"Legare","sequence":"first","affiliation":[{"name":"Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chengxin","family":"Liu","sequence":"additional","affiliation":[{"name":"Greenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richard M.","family":"Pauli","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Adekemi Yewande","family":"Alade","sequence":"additional","affiliation":[{"name":"Department of Epidemiology, Johns Hopkins University, Baltimore, Maryland;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S. Shahrukh","family":"Hashmi","sequence":"additional","affiliation":[{"name":"McGovern Medical School at University of Texas Health, Houston, Texas;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jeffrey W.","family":"Campbell","sequence":"additional","affiliation":[{"name":"A. I. duPont Hospital for Children, Thomas Jefferson University, Wilmington, Delaware; and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Cory J.","family":"Smid","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin;"},{"name":"Children\u2019s Wisconsin, Medical College of Wisconsin, Milwaukee, Wisconsin"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peggy","family":"Modaff","sequence":"additional","affiliation":[{"name":"Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mary Ellen","family":"Little","sequence":"additional","affiliation":[{"name":"A. I. duPont Hospital for Children, Thomas Jefferson University, Wilmington, Delaware; and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David F.","family":"Rodriguez-Buritica","sequence":"additional","affiliation":[{"name":"McGovern Medical School at University of Texas Health, Houston, Texas;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maria Elena","family":"Serna","sequence":"additional","affiliation":[{"name":"McGovern Medical School at University of Texas Health, Houston, Texas;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jaqueline T.","family":"Hecht","sequence":"additional","affiliation":[{"name":"McGovern Medical School at University of Texas Health, Houston, Texas;"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Julie E.","family":"Hoover-Fong","sequence":"additional","affiliation":[{"name":"Greenberg Center for Skeletal Dysplasias, McKusick-Nathans Department of Genetic Medicine, and"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Michael B.","family":"Bober","sequence":"additional","affiliation":[{"name":"A. I. duPont Hospital for Children, Thomas Jefferson University, Wilmington, Delaware; and"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1754","reference":[{"issue":"1","key":"b1","series-title":"Orphanet J Rare Dis","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1186\/s13023-018-0972-6","article-title":"Achondroplasia: a comprehensive clinical review","volume":"14","author":"Pauli RM","year":"2019","unstructured":"Pauli RM. Achondroplasia: a comprehensive clinical review. Orphanet J Rare Dis. 2019;14(1):1.3060619010.1186\/s13023-018-0972-6"},{"issue":"2","key":"b2","series-title":"Genet Med","doi-asserted-by":"publisher","first-page":"459","DOI":"10.1038\/s41436-018-0070-0","article-title":"Cervical spinal cord compression in infants with achondroplasia: should neuroimaging be routine?","volume":"21","author":"Sanders VR","year":"2019","unstructured":"Sanders VR, Sheldon SH, Charrow J. Cervical spinal cord compression in infants with achondroplasia: should neuroimaging be routine?. Genet Med. 2019;21(2):459\u2013463.10.1038\/s41436-018-0070-029872110"},{"issue":"2","key":"b3","series-title":"Am J Hum Genet","first-page":"368","article-title":"Achondroplasia is defined by recurrent G380R mutations of FGFR3","volume":"56","author":"Bellus GA","year":"1995","unstructured":"Bellus GA, Hefferon TW, Ortiz de Luna RI, . Achondroplasia is defined by recurrent G380R mutations of FGFR3. Am J Hum Genet. 1995;56(2):368\u2013373.7847369"},{"issue":"2","key":"b4","series-title":"Hum Mol Genet","doi-asserted-by":"publisher","first-page":"227","DOI":"10.1093\/hmg\/ddn339","article-title":"FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway","volume":"18","author":"Matsushita T","year":"2009","unstructured":"Matsushita T, Wilcox WR, Chan YY, . FGFR3 promotes synchondrosis closure and fusion of ossification centers through the MAPK pathway. Hum Mol Genet. 2009;18(2):227\u2013240.1892300310.1093\/hmg\/ddn339"},{"issue":"3","key":"b5","series-title":"Am J Hum Genet","first-page":"732","article-title":"Prospective assessment of risks for cervicomedullary-junction compression in infants with achondroplasia","volume":"56","author":"Pauli RM","year":"1995","unstructured":"Pauli RM, Horton VK, Glinski LP, Reiser CA. Prospective assessment of risks for cervicomedullary-junction compression in infants with achondroplasia. Am J Hum Genet. 1995;56(3):732\u2013744.7887429"},{"issue":"4","key":"b6","series-title":"J Pediatr","doi-asserted-by":"publisher","first-page":"522","DOI":"10.1016\/S0022-3476(87)80542-5","article-title":"Cervicomedullary compression in young patients with achondroplasia: value of comprehensive neurologic and respiratory evaluation","volume":"110","author":"Reid CS","year":"1987","unstructured":"Reid CS, Pyeritz RE, Kopits SE, . Cervicomedullary compression in young patients with achondroplasia: value of comprehensive neurologic and respiratory evaluation. J Pediatr. 1987;110(4):522\u2013530.10.1016\/S0022-3476(87)80542-53559799"},{"issue":"4","key":"b7","series-title":"Am J Hum Genet","first-page":"824","article-title":"Cervicomedullary junction compression in infants with achondroplasia: when to perform neurosurgical decompression","volume":"56","author":"Rimoin DL","year":"1995","unstructured":"Rimoin DL. Cervicomedullary junction compression in infants with achondroplasia: when to perform neurosurgical decompression. Am J Hum Genet. 1995;56(4):824\u2013827.7717392"},{"issue":"2","key":"b8","series-title":"Cell","doi-asserted-by":"publisher","first-page":"335","DOI":"10.1016\/0092-8674(94)90302-6","article-title":"Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia","volume":"78","author":"Shiang R","year":"1994","unstructured":"Shiang R, Thompson LM, Zhu YZ, . Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell. 1994;78(2):335\u2013342.791388310.1016\/0092-8674(94)90302-6"},{"issue":"3","key":"b9","series-title":"J Neurosurg","doi-asserted-by":"publisher","first-page":"375","DOI":"10.3171\/jns.1990.73.3.0375","article-title":"Craniocervical decompression for cervicomedullary compression in pediatric patients with achondroplasia","volume":"73","author":"Aryanpur J","year":"1990","unstructured":"Aryanpur J, Hurko O, Francomano C, . Craniocervical decompression for cervicomedullary compression in pediatric patients with achondroplasia. J Neurosurg. 1990;73(3):375\u2013382.238477510.3171\/jns.1990.73.3.0375"},{"issue":"3)(suppl","key":"b10","series-title":"J Neurosurg","first-page":"166","article-title":"Cervicomedullary decompression for foramen magnum stenosis in achondroplasia","volume":"104","author":"Bagley CA","year":"2006","unstructured":"Bagley CA, Pindrik JA, Bookland MJ, . Cervicomedullary decompression for foramen magnum stenosis in achondroplasia. J Neurosurg. 2006;104(3)(suppl):166\u2013172.16572633"},{"key":"b11","series-title":"Basic Life Sci","first-page":"207","article-title":"Surgical management of cervicomedullary compression in achondroplastic patients","volume":"48","author":"Carson B","year":"1988","unstructured":"Carson B, Winfield J, Wang H, . Surgical management of cervicomedullary compression in achondroplastic patients. Basic Life Sci. 1988;48:207\u2013214.3240255"},{"issue":"1","key":"b12","series-title":"J Neurosurg","doi-asserted-by":"publisher","first-page":"49","DOI":"10.3171\/jns.1981.54.1.0049","article-title":"Neurological manifestations of pediatric achondroplasia","volume":"54","author":"Yamada H","year":"1981","unstructured":"Yamada H, Nakamura S, Tajima M, Kageyama N. Neurological manifestations of pediatric achondroplasia. J Neurosurg. 1981;54(1):49\u201357.746312010.3171\/jns.1981.54.1.0049"},{"issue":"4","key":"b13","series-title":"Dev Med Child Neurol","doi-asserted-by":"publisher","first-page":"489","DOI":"10.1111\/j.1469-8749.1982.tb13654.x","article-title":"Unexpected death of children with achondroplasia after the perinatal period","volume":"24","author":"Bland JD","year":"1982","unstructured":"Bland JD, Emery JL. Unexpected death of children with achondroplasia after the perinatal period. Dev Med Child Neurol. 1982;24(4):489\u2013492.10.1111\/j.1469-8749.1982.tb13654.x7117707"},{"issue":"3","key":"b14","series-title":"J Pediatr","doi-asserted-by":"publisher","first-page":"398","DOI":"10.1016\/S0022-3476(84)81103-8","article-title":"Apnea as the sole manifestation of cord compression in achondroplasia","volume":"104","author":"Fremion AS","year":"1984","unstructured":"Fremion AS, Garg BP, Kalsbeck J. Apnea as the sole manifestation of cord compression in achondroplasia. J Pediatr. 1984;104(3):398\u2013401.670779510.1016\/S0022-3476(84)81103-8"},{"issue":"3","key":"b15","series-title":"J Pediatr","doi-asserted-by":"publisher","first-page":"342","DOI":"10.1016\/S0022-3476(84)81092-6","article-title":"Apnea and sudden unexpected death in infants with achondroplasia","volume":"104","author":"Pauli RM","year":"1984","unstructured":"Pauli RM, Scott CI, Wassman ER Jr, . Apnea and sudden unexpected death in infants with achondroplasia. J Pediatr. 1984;104(3):342\u2013348.10.1016\/S0022-3476(84)81092-66707788"},{"issue":"11","key":"b16","series-title":"Am J Med Gent A","doi-asserted-by":"publisher","first-page":"2359","DOI":"10.1002\/ajmg.a.40528","article-title":"Multicenter study of mortality in achondroplasia","volume":"176","author":"Hashmi SS","year":"2018","unstructured":"Hashmi SS, Gamble C, Hoover-Fong J. Multicenter study of mortality in achondroplasia. Am J Med Gent A. 2018;176(11):2359\u20132364.10.1002\/ajmg.a.40528"},{"key":"b17","series-title":"Genet Med","article-title":"Achondroplasia Natural History Study (CLARITY): a multicenter retrospective cohort study of achondroplasia in the United States","author":"Hoover-Fong JE","unstructured":"Hoover-Fong JE, Alade AY, Hashmi SS, . Achondroplasia Natural History Study (CLARITY): a multicenter retrospective cohort study of achondroplasia in the United States. Genet Med. Published online May 18, 2021. doi:10.1038\/s41436-021-01165-234006999"},{"key":"b18","article-title":"Achondroplasia, a 15-year retrospective review of outcomes in 110 French pediatric patients","author":"Baujat G","unstructured":"Baujat G, Michot C, Fauroux B. Achondroplasia, a 15-year retrospective review of outcomes in 110 French pediatric patients. Poster presented at: 14th International Skeletal Dysplasia Society Meeting. September 11\u201314, 2019;Oslo, Norway."},{"issue":"3","key":"b19","series-title":"Am J Hum Genet","first-page":"454","article-title":"Mortality in achondroplasia","volume":"41","author":"Hecht JT","year":"1987","unstructured":"Hecht JT, Francomano CA, Horton WA, Annegers JF. Mortality in achondroplasia. Am J Hum Genet. 1987;41(3):454\u2013464.3631079"},{"issue":"2","key":"b20","series-title":"Am J Med Genet","doi-asserted-by":"publisher","first-page":"355","DOI":"10.1002\/ajmg.1320200219","article-title":"Computerized tomography of the foramen magnum: achondroplastic values compared to normal standards","volume":"20","author":"Hecht JT","year":"1985","unstructured":"Hecht JT, Nelson FW, Butler IJ, . Computerized tomography of the foramen magnum: achondroplastic values compared to normal standards. Am J Med Genet. 1985;20(2):355\u2013360.10.1002\/ajmg.13202002193976726"},{"issue":"4","key":"b21","series-title":"Am J Med Genet","doi-asserted-by":"publisher","first-page":"528","DOI":"10.1002\/ajmg.1320320421","article-title":"Growth of the foramen magnum in achondroplasia","volume":"32","author":"Hecht JT","year":"1989","unstructured":"Hecht JT, Horton WA, Reid CS, . Growth of the foramen magnum in achondroplasia. Am J Med Genet. 1989;32(4):528\u2013535.277399810.1002\/ajmg.1320320421"},{"issue":"2","key":"b22","series-title":"Am J Med Genet A","doi-asserted-by":"publisher","first-page":"163","DOI":"10.1002\/ajmg.a.30342","article-title":"Living with achondroplasia: quality of life evaluation following cervico-medullary decompression","volume":"131","author":"Ho NC","year":"2004","unstructured":"Ho NC, Guarnieri M, Brant LJ, . Living with achondroplasia: quality of life evaluation following cervico-medullary decompression. Am J Med Genet A. 2004;131(2):163\u2013167.1548700810.1002\/ajmg.a.30342"}],"container-title":["Journal of Neurosurgery: Pediatrics"],"original-title":[],"link":[{"URL":"https:\/\/thejns.org\/view\/journals\/j-neurosurg-pediatr\/28\/2\/article-p229.xml","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/thejns.org\/downloadpdf\/journals\/j-neurosurg-pediatr\/28\/2\/article-p229.xml","content-type":"text\/html","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/thejns.org\/downloadpdf\/journals\/j-neurosurg-pediatr\/28\/2\/article-p229.xml","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,11,14]],"date-time":"2026-11-14T01:54:27Z","timestamp":1794621267000},"score":1,"resource":{"primary":{"URL":"https:\/\/thejns.org\/view\/journals\/j-neurosurg-pediatr\/28\/2\/article-p229.xml"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2021,8]]},"references-count":22,"journal-issue":{"issue":"2"},"URL":"https:\/\/doi.org\/10.3171\/2020.12.peds20715","relation":{},"ISSN":["1933-0707","1933-0715"],"issn-type":[{"value":"1933-0707","type":"print"},{"value":"1933-0715","type":"electronic"}],"subject":[],"published":{"date-parts":[[2021,8]]}}}