{"title":"儿童胸膜炎和根状软骨发育不良Puctata的肋间间隙骨化","authors":"J. Tan, Chor Lip Henry Tan, S. Vendargon","doi":"10.21699/ajcr.v9i1.670","DOIUrl":null,"url":null,"abstract":"Rhizomelic chondrodysplasia punctata (RCDP) is an autosomal recessive metabolic disorder characterised by symmetric rhizomelic shortening of limbs and skeletal anomalies, dwarfism, microcephaly, micrognathia, cleft palate, ichthyosis, congenital heart disease, seizures, repeated respiratory infections, congenital cataracts, and deafness.[1,2] We report a case of RCDP with empyema thoracis and ossification of intercostal spaces.","PeriodicalId":89657,"journal":{"name":"APSP journal of case reports","volume":"9 1","pages":"5"},"PeriodicalIF":0.0000,"publicationDate":"2018-03-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Intercostal Space Ossification in a Child with Empyema Thoracis and Rhizomelic Chondrodysplasia Punctata\",\"authors\":\"J. Tan, Chor Lip Henry Tan, S. Vendargon\",\"doi\":\"10.21699/ajcr.v9i1.670\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Rhizomelic chondrodysplasia punctata (RCDP) is an autosomal recessive metabolic disorder characterised by symmetric rhizomelic shortening of limbs and skeletal anomalies, dwarfism, microcephaly, micrognathia, cleft palate, ichthyosis, congenital heart disease, seizures, repeated respiratory infections, congenital cataracts, and deafness.[1,2] We report a case of RCDP with empyema thoracis and ossification of intercostal spaces.\",\"PeriodicalId\":89657,\"journal\":{\"name\":\"APSP journal of case reports\",\"volume\":\"9 1\",\"pages\":\"5\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-03-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"APSP journal of case reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21699/ajcr.v9i1.670\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"APSP journal of case reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21699/ajcr.v9i1.670","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Intercostal Space Ossification in a Child with Empyema Thoracis and Rhizomelic Chondrodysplasia Punctata
Rhizomelic chondrodysplasia punctata (RCDP) is an autosomal recessive metabolic disorder characterised by symmetric rhizomelic shortening of limbs and skeletal anomalies, dwarfism, microcephaly, micrognathia, cleft palate, ichthyosis, congenital heart disease, seizures, repeated respiratory infections, congenital cataracts, and deafness.[1,2] We report a case of RCDP with empyema thoracis and ossification of intercostal spaces.