Literature DB >> 11529636

A severely disabling disorder: fibrodysplasia ossificans progressiva.

H Kocyigit1, N Hizli, A Memis, D Sabah, A Memis.   

Abstract

Fibrodysplasia ossificans progressiva (FOP) is an extremely rare hereditary disorder characterised by progressive heterotopic ossification of the soft tissues. The resulting progressive immobilisation of the limbs, jaw and chest wall generally leads to severe disability. We present an 18-year-old girl with advanced FOP. She had three operative interventions to excise her ectopic bones but all resulted in failure. Treatment strategies for this disorder should include the avoidance of exacerbating factors.

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Year:  2001        PMID: 11529636     DOI: 10.1007/s100670170044

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  2 in total

1.  Fibrodysplasia ossificans progressiva in a Malian boy of Bamako.

Authors:  Moussa Traore; Jeannette Traore Thomas; Cheick Oumar Guinto; Mamady Kane; Siona Traore
Journal:  Clin Rheumatol       Date:  2004-12       Impact factor: 2.980

2.  When Limb Surgery Has Become the Only Life-Saving Therapy in FOP: A Case Report and Systematic Review of the Literature.

Authors:  Esmée Botman; Sanne Treurniet; Wouter D Lubbers; Lothar A Schwarte; Patrick R Schober; Louise Sabelis; Edgar J G Peters; Annelies van Schie; Ralph de Vries; Zvi Grunwald; Bernard J Smilde; Jakko A Nieuwenhuijzen; Marieke Visser; Dimitra Micha; Nathalie Bravenboer; J Coen Netelenbos; Bernd P Teunissen; Pim de Graaf; Pieter G H M Raijmakers; Jan Maerten Smit; Elisabeth M W Eekhoff
Journal:  Front Endocrinol (Lausanne)       Date:  2020-08-21       Impact factor: 5.555

  2 in total

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