Literature DB >> 9133349

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

D Sillence1, S Worthington, J Dixon, R Osborn, K Kozlowski.   

Abstract

The clinical, radiographic, and morphological findings in 25 cases of atelosteogenesis and boomerang dysplasia have been reviewed. The review confirms the nosologic grouping of atelosteogenesis type I with boomerang dysplasia and the clinical and radiographic overlap of features between atel- osteogenesis I and atelosteogene- sis II (synonymous with De la Chapelle dysplasia) and a group of patients with atelosteogenesis type III. A common pathogenesis is suggested for atelosteogenesis type I and boomerang dysplasia. A marked excess of male fetuses with boomerang dysplasia was observed. Atelosteogenesis type II shows distinctive chondro-osseous histopathology with a major disturbance in cartilage matrix macromolecules. An overlap of phenotypic, radiographic, morphological, and cartilage histochemical features with those observed in diastrophic dysplasia and achondrogenesis type IB suggests that atelosteogenesis type II has common pathogenetic features with disorders of sulfation of connective tissue matrix macro- molecules.

Entities:  

Mesh:

Year:  1997        PMID: 9133349     DOI: 10.1007/s002470050154

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


  7 in total

1.  A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.

Authors:  Louise S Bicknell; Claire Farrington-Rock; Yousef Shafeghati; Patrick Rump; Yasemin Alanay; Yves Alembik; Navid Al-Madani; Helen Firth; Mohammad Hassan Karimi-Nejad; Chong Ae Kim; Kathryn Leask; Melissa Maisenbacher; Ellen Moran; John G Pappas; Paolo Prontera; Thomy de Ravel; Jean-Pierre Fryns; Elizabeth Sweeney; Alan Fryer; Sheila Unger; L C Wilson; Ralph S Lachman; David L Rimoin; Daniel H Cohn; Deborah Krakow; Stephen P Robertson
Journal:  J Med Genet       Date:  2006-06-26       Impact factor: 6.318

2.  Mutations responsible for Larsen syndrome cluster in the FLNB protein.

Authors:  D Zhang; J A Herring; S S Swaney; T B McClendon; X Gao; R H Browne; K E Rathjen; C E Johnston; S Harris; N M Cain; C A Wise
Journal:  J Med Genet       Date:  2006-05       Impact factor: 6.318

Review 3.  A framework for the radiologic diagnosis of skeletal dysplasias and syndromes as revealed by molecular genetics.

Authors:  Jerry R Dwek
Journal:  Pediatr Radiol       Date:  2019-11-04

Review 4.  Recessive omodysplasia: five new cases and review of the literature.

Authors:  Nursel H Elçioglu; Karl H Gustavson; Andrew O M Wilkie; Memune Yüksel-Apak; Jürgen W Spranger
Journal:  Pediatr Radiol       Date:  2003-10-18

5.  Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibit.

Authors:  Helga Rehder; Franco Laccone; Susanne G Kircher; Ralf L Schild; Christiane Rapp; Rainer Bald; Bernt Schulze; Jana Behunova; Juergen Neesen; Katharina Schoner
Journal:  Am J Med Genet A       Date:  2018-05-23       Impact factor: 2.802

6.  Deciphering the Role of Filamin B Calponin-Homology Domain in Causing the Larsen Syndrome, Boomerang Dysplasia, and Atelosteogenesis Type I Spectrum Disorders via a Computational Approach.

Authors:  Udhaya Kumar S; Srivarshini Sankar; Salma Younes; Thirumal Kumar D; Muneera Naseer Ahmad; Sarah Samer Okashah; Balu Kamaraj; Abeer Mohammed Al-Subaie; George Priya Doss C; Hatem Zayed
Journal:  Molecules       Date:  2020-11-26       Impact factor: 4.411

7.  Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients.

Authors:  Katta Mohan Girisha; Abdul Mueed Bidchol; Luitgard Graul-Neumann; Ashish Gupta; Ute Hehr; Davor Lessel; Sean Nader; Hitesh Shah; Julia Wickert; Kerstin Kutsche
Journal:  BMC Med Genet       Date:  2016-04-06       Impact factor: 2.103

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.