Fibrodysplasia ossificans progressiva in a young adult with genetic mutation
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference22 articles.
1. Early diagnosis of fibrodysplasia ossificans progressiva;Kaplan;Pediatrics,2008
2. Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1;Kaplan;Hum Mutat,2009
3. Fibrodysplasia ossificans progressiva: a current review of imaging findings;Bauer;Skeletal Radiol,2018
4. Iatrogenic harm caused by diagnostic errors in fibrodysplasia ossificans progressiva;Kitterman;Pediatrics,2005
5. A recurrent mutation c.617G>A in the ACVR1 gene causes fibrodysplasia ossificans progressiva in two Chinese patients;Sun;Calcif Tissue Int,2009
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Knowledge and awareness about fibrodysplasia ossificans progressiva among dental students;J ADV PHARM TECHNOL;2022
2. Fibrodysplasia ossificans progressiva: A rare disease with spinal deformity and severe hip dysfunction;Frontiers in Pediatrics;2022-09-15
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