{"title":"全麻下儿童线粒体肌病的牙科治疗","authors":"Saime Esin Güney, C. Araz, S. Çehreli","doi":"10.5336/CASEREP.2018-60898","DOIUrl":null,"url":null,"abstract":"178 itochondrial myopathies (MM) are uncommon disorders caused by structural and functional abnormalities in mitochondria due to inquietation of the mitochondrial chain of respiration or oxidative phosphorylation.1,2 The condition occurs with an incidence of 1 per 4-5000 live births.3 Primary “target” organs are the central nervous system and the liver but the disorder may account for a wider range of neurologic, endocrine disorders as well as cardiac complications.","PeriodicalId":23460,"journal":{"name":"Türkiye Klinikleri Journal of Case Reports","volume":"18 1","pages":"178-181"},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dental Treatment of a Child with Mitochondrial Myopathy Under General Anesthesia\",\"authors\":\"Saime Esin Güney, C. Araz, S. Çehreli\",\"doi\":\"10.5336/CASEREP.2018-60898\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"178 itochondrial myopathies (MM) are uncommon disorders caused by structural and functional abnormalities in mitochondria due to inquietation of the mitochondrial chain of respiration or oxidative phosphorylation.1,2 The condition occurs with an incidence of 1 per 4-5000 live births.3 Primary “target” organs are the central nervous system and the liver but the disorder may account for a wider range of neurologic, endocrine disorders as well as cardiac complications.\",\"PeriodicalId\":23460,\"journal\":{\"name\":\"Türkiye Klinikleri Journal of Case Reports\",\"volume\":\"18 1\",\"pages\":\"178-181\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Türkiye Klinikleri Journal of Case Reports\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5336/CASEREP.2018-60898\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Türkiye Klinikleri Journal of Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5336/CASEREP.2018-60898","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Dental Treatment of a Child with Mitochondrial Myopathy Under General Anesthesia
178 itochondrial myopathies (MM) are uncommon disorders caused by structural and functional abnormalities in mitochondria due to inquietation of the mitochondrial chain of respiration or oxidative phosphorylation.1,2 The condition occurs with an incidence of 1 per 4-5000 live births.3 Primary “target” organs are the central nervous system and the liver but the disorder may account for a wider range of neurologic, endocrine disorders as well as cardiac complications.
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