Literature DB >> 3155744

The prevalence of skeletal dysplasias. An estimate of their minimum frequency and the number of patients requiring orthopaedic care.

R Wynne-Davies, J Gormley.   

Abstract

An attempt has been made to estimate the number of living people with skeletal dysplasias (osteochondrodysplasias) in Scotland, England and Wales, ascertained through five orthopaedic centres in different parts of Britain. Index patients and their affected relatives were sought and reassessed. Over the 30-year period between 1950 and 1979 inclusive a minimum prevalence was calculated (excluding stillbirths, perinatal deaths, and patients with chromosome anomalies, metabolic bone disease and short stature per se). The results indicate that there were in the community upwards of 10 000 individuals, at various ages over this period, with these largely genetic disorders. A more accurate estimate is of some 6000 of them requiring substantial orthopaedic care, and who were physically handicapped throughout life, about half of them severely so.

Entities:  

Mesh:

Year:  1985        PMID: 3155744

Source DB:  PubMed          Journal:  J Bone Joint Surg Br        ISSN: 0301-620X


  26 in total

1.  The molecular basis of X-linked spondyloepiphyseal dysplasia tarda.

Authors:  A K Gedeon; G E Tiller; M Le Merrer; S Heuertz; L Tranebjaerg; D Chitayat; S Robertson; I A Glass; R Savarirayan; W G Cole; D L Rimoin; B G Kousseff; H Ohashi; B Zabel; A Munnich; J Gecz; J C Mulley
Journal:  Am J Hum Genet       Date:  2001-05-08       Impact factor: 11.025

2.  A report of an Indian boy with a delayed diagnosis of pseudochondroplasia.

Authors:  Ankur Singh; T Abiramalatha; Gaurav Pradhan; Dong-Kyu Jin; Seema Kapoor
Journal:  J Clin Diagn Res       Date:  2013-07-01

3.  A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tarda.

Authors:  G E Tiller; V L Hannig; D Dozier; L Carrel; K C Trevarthen; W R Wilcox; S Mundlos; J L Haines; A K Gedeon; J Gecz
Journal:  Am J Hum Genet       Date:  2001-04-26       Impact factor: 11.025

4.  Structural and segregation analysis of the type II collagen gene (COL2A1) in some heritable chondrodysplasias.

Authors:  P Wordsworth; D Ogilvie; L Priestley; R Smith; R Wynne-Davies; B Sykes
Journal:  J Med Genet       Date:  1988-08       Impact factor: 6.318

5.  Congenital generalised bone dysplasias: a clinical, radiological, and epidemiological survey.

Authors:  P E Andersen; M Hauge
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

6.  Progressive pseudorheumatoid chondrodysplasia: a report of nine cases in three families.

Authors:  H Rezai-Delui; G Mamoori; E Sadri-Mahvelati; N M Noori
Journal:  Skeletal Radiol       Date:  1994-08       Impact factor: 2.199

7.  Is webbing (pterygia) a constant feature in patients with Escobar syndrome?

Authors:  Ali Al Kaissi; Vladimir Kenis; Sergey Laptiev; Maher Ben Ghachem; Klaus Klaushofer; Rudolf Ganger; Franz Grill
Journal:  Orthop Surg       Date:  2013-11       Impact factor: 2.071

Review 8.  Mechanisms that drive bone pain across the lifespan.

Authors:  Patrick W Mantyh
Journal:  Br J Clin Pharmacol       Date:  2018-11-22       Impact factor: 4.335

9.  Melorheostosis: A Clinical, Pathologic, and Radiologic Case Series.

Authors:  Cameron N Fick; Nadja Fratzl-Zelman; Paul Roschger; Klaus Klaushofer; Smita Jha; Joan C Marini; Timothy Bhattacharyya
Journal:  Am J Surg Pathol       Date:  2019-11       Impact factor: 6.394

Review 10.  Melorheostosis: a Rare Sclerosing Bone Dysplasia.

Authors:  Anupam Kotwal; Bart L Clarke
Journal:  Curr Osteoporos Rep       Date:  2017-08       Impact factor: 5.096

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.