{"title":"进行性骨化性纤维发育不良-一种罕见的牙关原因","authors":"Ravi Sankaran, S. Nampoothiri, A. Bhaskaran","doi":"10.4103/ijpmr.ijpmr_3_22","DOIUrl":null,"url":null,"abstract":"Fibrodysplasia ossificans progressiva (FOP) is a progressively disabling genetic disorder. It is characterised by development of a secondary skeleton due to progressive hypertrophic ossification. It causes immobility through progressive conversion of skeletal muscle and soft connective tissue into a second skeleton of heterotopic bone. Approximately 1 in 2 million children worldwide are diagnosed with FOP. We present the case of a person erroneously referred for physical therapy of trismus.","PeriodicalId":220492,"journal":{"name":"Indian Journal of Physical Medicine & Rehabilitation","volume":"19 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Fibrodysplasia ossificans progressiva - An uncommon cause of trismus\",\"authors\":\"Ravi Sankaran, S. Nampoothiri, A. Bhaskaran\",\"doi\":\"10.4103/ijpmr.ijpmr_3_22\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Fibrodysplasia ossificans progressiva (FOP) is a progressively disabling genetic disorder. It is characterised by development of a secondary skeleton due to progressive hypertrophic ossification. It causes immobility through progressive conversion of skeletal muscle and soft connective tissue into a second skeleton of heterotopic bone. Approximately 1 in 2 million children worldwide are diagnosed with FOP. We present the case of a person erroneously referred for physical therapy of trismus.\",\"PeriodicalId\":220492,\"journal\":{\"name\":\"Indian Journal of Physical Medicine & Rehabilitation\",\"volume\":\"19 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Indian Journal of Physical Medicine & Rehabilitation\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4103/ijpmr.ijpmr_3_22\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Indian Journal of Physical Medicine & Rehabilitation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4103/ijpmr.ijpmr_3_22","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Fibrodysplasia ossificans progressiva - An uncommon cause of trismus
Fibrodysplasia ossificans progressiva (FOP) is a progressively disabling genetic disorder. It is characterised by development of a secondary skeleton due to progressive hypertrophic ossification. It causes immobility through progressive conversion of skeletal muscle and soft connective tissue into a second skeleton of heterotopic bone. Approximately 1 in 2 million children worldwide are diagnosed with FOP. We present the case of a person erroneously referred for physical therapy of trismus.
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