Literature DB >> 2368807

Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II.

H J Stern1, J M Graham, R S Lachman, W Horton, P M Bernini, P K Spiegel, J Bodurtha, E J Ives, M Bocian, D L Rimoin.   

Abstract

We present 5 cases of a short-limb dwarfism syndrome whose manifestations overlap those of atelosteogenesis and oto-palato-digital syndrome Type II. Clinical, radiographic, genetic, and histologic data are presented which demonstrate differences between our patients and previously reported cases of these other conditions. We conclude that the disorder seen in these children represents a distinct chondrodysplasia for which we propose the name atelosteogenesis Type III.

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Year:  1990        PMID: 2368807     DOI: 10.1002/ajmg.1320360212

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  8 in total

1.  Otopalatodigital syndrome type II.

Authors:  S E Holder; R M Winter
Journal:  J Med Genet       Date:  1993-04       Impact factor: 6.318

Review 2.  Atelosteogenesis type 2.

Authors:  R Newbury-Ecob
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

3.  Oto-palato-digital syndrome type II. Report of two related cases.

Authors:  P W Gendall; K Kozlowski
Journal:  Pediatr Radiol       Date:  1992

4.  Occipital projections in the skeletal dysplasias.

Authors:  Yuji Takamine; Ralph S Lachman; Fiona M Field; David L Rimoin
Journal:  Pediatr Radiol       Date:  2004-04-24

Review 5.  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

6.  Atelosteogenesis type II is caused by mutations in the diastrophic dysplasia sulfate-transporter gene (DTDST): evidence for a phenotypic series involving three chondrodysplasias.

Authors:  J Hästbacka; A Superti-Furga; W R Wilcox; D L Rimoin; D H Cohn; E S Lander
Journal:  Am J Hum Genet       Date:  1996-02       Impact factor: 11.025

7.  Atelosteogenesis type III: a case report.

Authors:  M J Fallon; A Hockey; L A Hallam
Journal:  Pediatr Radiol       Date:  1994

8.  Identification of a de novo heterozygous missense FLNB mutation in lethal atelosteogenesis type I by exome sequencing.

Authors:  Ga Won Jeon; Mi-Na Lee; Ji Mi Jung; Seong Yeon Hong; Young Nam Kim; Jong Beom Sin; Chang-Seok Ki
Journal:  Ann Lab Med       Date:  2014-02-13       Impact factor: 3.464

  8 in total

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