S. Ryabykh, P. Ochirova, M. Shboul, Alexander B Gubin, A. Burtsev, M. Saifutdinov, S. Kircher, A. Kaissi
{"title":"Distinctive Spine Deformities in Patients with Hurler (IH) and Hurler-Scheie (I-H/S) Syndrome","authors":"S. Ryabykh, P. Ochirova, M. Shboul, Alexander B Gubin, A. Burtsev, M. Saifutdinov, S. Kircher, A. Kaissi","doi":"10.46889/josr.2021.2304","DOIUrl":null,"url":null,"abstract":"Purpose: Progressive kyphoscoliosis is not of uncommon occurrence in patients with MPSs. Cranio-cervical junction in patients with MPSs are under the threat of three life threatening elements, namely GAGs accumulation, C1-2 instability, and progressive cervical vascular abnormalities. Material and Methods: Seven patients’ two girls and five boys with age range from 3 to 9 years presented with progressive kyphoscoliosis and atlanto-axial instability. Phenotype/genotype confirmed the diagnosis of Hurler syndrome and Hurler-Scheie syndrome. Though, spine deformities were to a certain extent similar in both types but with different age of onset. Results: Children with kyphoscoliosis of apical Cobb’s angle ranging between 60/65° were corrected up to 5° with normal sagittal spine balance. All showed an improvement in the neurological and functional status of Frankel motor scale (PreOp C / PostOp D) and Nurick scale (PreOp 2-3 / PostOp 2-3). The severity of myelopathy on the mJOA scale decreased (PreOp 12 / PostOp 10). Three children were excluded from surgical interventions because","PeriodicalId":382112,"journal":{"name":"Journal of Orthopaedic Science and Research","volume":"29 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Orthopaedic Science and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.46889/josr.2021.2304","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose: Progressive kyphoscoliosis is not of uncommon occurrence in patients with MPSs. Cranio-cervical junction in patients with MPSs are under the threat of three life threatening elements, namely GAGs accumulation, C1-2 instability, and progressive cervical vascular abnormalities. Material and Methods: Seven patients’ two girls and five boys with age range from 3 to 9 years presented with progressive kyphoscoliosis and atlanto-axial instability. Phenotype/genotype confirmed the diagnosis of Hurler syndrome and Hurler-Scheie syndrome. Though, spine deformities were to a certain extent similar in both types but with different age of onset. Results: Children with kyphoscoliosis of apical Cobb’s angle ranging between 60/65° were corrected up to 5° with normal sagittal spine balance. All showed an improvement in the neurological and functional status of Frankel motor scale (PreOp C / PostOp D) and Nurick scale (PreOp 2-3 / PostOp 2-3). The severity of myelopathy on the mJOA scale decreased (PreOp 12 / PostOp 10). Three children were excluded from surgical interventions because