Literature DB >> 15226573

Fibrodysplasia ossificans progressiva.

L Subramanyam1, Kalpana Gowrishankar, So Shivbalan, A Balachandran.   

Abstract

A 2-year-old boy presented with low-grade fever and multiple progressive painful swellings over upper dorsal trunk and supraclavicular region with progressive stiffening of skin for the last 2 months. Examination revealed dysmorphic face, proximally placed thumb and bilateral hallux valgus. Hence, a diagnosis of Fibrodysplasia Ossificans Progressiva was entertained.

Entities:  

Mesh：

Year:  2004        PMID： 15226573     DOI： 10.1007/bf02724306

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


  5 in total

1.  Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31.

Authors:  G Feldman; M Li; S Martin; M Urbanek; J A Urtizberea; M Fardeau; M LeMerrer; J M Connor; J Triffitt; R Smith; M Muenke; F S Kaplan; E M Shore
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Genetic aspects of fibrodysplasia ossificans progressiva.

Authors:  J M Connor; D A Evans
Journal:  J Med Genet       Date:  1982-02       Impact factor: 6.318

3.  Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva.

Authors:  A B Shafritz; E M Shore; F H Gannon; M A Zasloff; R Taub; M Muenke; F S Kaplan
Journal:  N Engl J Med       Date:  1996-08-22       Impact factor: 91.245

4.  Fibrodysplasia ossificans progressiva. The clinical features and natural history of 34 patients.

Authors:  J M Connor; D A Evans
Journal:  J Bone Joint Surg Br       Date:  1982

5.  The histopathology of fibrodysplasia ossificans progressiva. An endochondral process.

Authors:  F S Kaplan; J A Tabas; F H Gannon; G Finkel; G V Hahn; M A Zasloff
Journal:  J Bone Joint Surg Am       Date:  1993-02       Impact factor: 5.284
  5 in total
  1 in total

1.  Sporadic Fibrodysplasia Ossificans Progressiva in an Egyptian Infant with c.617G > A Mutation in ACVR1 Gene: A Case Report and Review of Literature.

Authors:  Mohammad Al-Haggar; Nermin Ahmad; Sohier Yahia; Amany Shams; Bothina Hasaneen; Rasha Hassan Hassan; Yahya Wahba; Nanees Abdel-Badie Salem; Dina Abdel-Hady
Journal:  Case Rep Genet       Date:  2013-01-23
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.