Literature DB >> 31686164

A framework for the radiologic diagnosis of skeletal dysplasias and syndromes as revealed by molecular genetics.

Jerry R Dwek1.   

Abstract

This article simplifies the radiologic diagnosis of skeletal dysplasia by first presenting an ordered approach for analysis of standard radiographs done for skeletal dysplasias. With that foundation, a more detailed discussion of three separate families of skeletal disorders follows. Similarities among dysplasia group members are discussed to provide a certain connectedness among dysplasias. The paper also elucidates the scientific basis behind the radiographic findings so that previously purely descriptive terms have the weight of understanding behind them.

Entities:  

Keywords:  Children; Dysplasia; Molecular genetics; Radiography; Skeleton

Mesh:

Year:  2019        PMID: 31686164     DOI: 10.1007/s00247-019-04545-8

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  15 in total

Review 1.  Radiological diagnosis of the constitutional disorders of bone. As easy as A, B, C?

Authors:  Amaka C Offiah; Christine M Hall
Journal:  Pediatr Radiol       Date:  2002-12-20

Review 2.  Atelosteogenesis syndromes: a review, with comments on their pathogenesis.

Authors:  D Sillence; S Worthington; J Dixon; R Osborn; K Kozlowski
Journal:  Pediatr Radiol       Date:  1997-05

3.  Diastrophic dwarfism.

Authors:  H TAYBI
Journal:  Radiology       Date:  1963-01       Impact factor: 11.105

4.  Ossification of the vertebral column in human foetuses: histological and computed tomography studies.

Authors:  A Skórzewska; M Grzymisławska; M Bruska; J Lupicka; W Woźniak
Journal:  Folia Morphol (Warsz)       Date:  2013-08       Impact factor: 1.183

Review 5.  Achondroplasia: Development, pathogenesis, and therapy.

Authors:  David M Ornitz; Laurence Legeai-Mallet
Journal:  Dev Dyn       Date:  2017-03-02       Impact factor: 3.780

6.  The vertebral body: radiographic configurations in various congenital and acquired disorders.

Authors:  R Kumar; F C Guinto; J E Madewell; L E Swischuk; R David
Journal:  Radiographics       Date:  1988-05       Impact factor: 5.333

7.  Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene.

Authors:  A Superti-Furga; J Hästbacka; W R Wilcox; D H Cohn; H J van der Harten; A Rossi; N Blau; D L Rimoin; B Steinmann; E S Lander; R Gitzelmann
Journal:  Nat Genet       Date:  1996-01       Impact factor: 38.330

Review 8.  The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.

Authors:  Z Vajo; C A Francomano; D J Wilkin
Journal:  Endocr Rev       Date:  2000-02       Impact factor: 19.871

Review 9.  Imaging of Skeletal Disorders Caused by Fibroblast Growth Factor Receptor Gene Mutations.

Authors:  Kiran M Sargar; Achint K Singh; Simon C Kao
Journal:  Radiographics       Date:  2017-10       Impact factor: 5.333

Review 10.  Nosology and classification of genetic skeletal disorders: 2010 revision.

Authors:  Matthew L Warman; Valerie Cormier-Daire; Christine Hall; Deborah Krakow; Ralph Lachman; Martine LeMerrer; Geert Mortier; Stefan Mundlos; Gen Nishimura; David L Rimoin; Stephen Robertson; Ravi Savarirayan; David Sillence; Juergen Spranger; Sheila Unger; Bernhard Zabel; Andrea Superti-Furga
Journal:  Am J Med Genet A       Date:  2011-03-15       Impact factor: 2.802

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  1 in total

Review 1.  International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia.

Authors:  Ravi Savarirayan; Penny Ireland; Melita Irving; Dominic Thompson; Inês Alves; Wagner A R Baratela; James Betts; Michael B Bober; Silvio Boero; Jenna Briddell; Jeffrey Campbell; Philippe M Campeau; Patricia Carl-Innig; Moira S Cheung; Martyn Cobourne; Valérie Cormier-Daire; Muriel Deladure-Molla; Mariana Del Pino; Heather Elphick; Virginia Fano; Brigitte Fauroux; Jonathan Gibbins; Mari L Groves; Lars Hagenäs; Therese Hannon; Julie Hoover-Fong; Morrys Kaisermann; Antonio Leiva-Gea; Juan Llerena; William Mackenzie; Kenneth Martin; Fabio Mazzoleni; Sharon McDonnell; Maria Costanza Meazzini; Josef Milerad; Klaus Mohnike; Geert R Mortier; Amaka Offiah; Keiichi Ozono; John A Phillips; Steven Powell; Yosha Prasad; Cathleen Raggio; Pablo Rosselli; Judith Rossiter; Angelo Selicorni; Marco Sessa; Mary Theroux; Matthew Thomas; Laura Trespedi; David Tunkel; Colin Wallis; Michael Wright; Natsuo Yasui; Svein Otto Fredwall
Journal:  Nat Rev Endocrinol       Date:  2021-11-26       Impact factor: 47.564

  1 in total

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