Fibrodysplasia Ossificans Progressiva: A Case Report

  • Sudeep Acharya Department of Oral and Maxillofacial Surgery, KIST Medical College and Teaching Hospital, Imadole, Lalitpur, Nepal
  • Sandhya Joshi Maxillofacial Unit, National Academy of Medical Science, National Trauma Center, Mahankal, Kathmandu, Nepal,
  • Rajib Chaulagain Department of Oral Pathology, KIST Medical College and Teaching Hospital, Imadole, Lalitpur, Nepal

Abstract

Fibrodysplasia ossificans progressiva is a genetic disorder of the connective tissue differentiation characterized by congenital malformation of the big toes and progressive heterotopic ossification in the extra skeletal tissues like tendons, ligaments, fascia and skeletal muscles leading to permanent disability. The prevalence is one in two million people. During childhood, it may be asymptomatic but in later life, progressive stiffness of major joints renders movement of the individual impossible. Currently, there is no effective treatment for this debilitating disease. Here, we present a case of 27 year old male with clinical and radiological features of fibrodysplasia ossificans progressiva.
Keywords: Fibrodysplasia ossificans progressive; heterotopic ossification; myositis ossificans; myositis ossificans progressive.

Published
2018-07-04
How to Cite
ACHARYA, Sudeep; JOSHI, Sandhya; CHAULAGAIN, Rajib. Fibrodysplasia Ossificans Progressiva: A Case Report. Journal of Nepal Health Research Council, [S.l.], v. 16, n. 2, p. 245-247, july 2018. ISSN 1999-6217. Available at: <http://jnhrc.com.np/index.php/jnhrc/article/view/1193>. Date accessed: 17 aug. 2018.