Literature DB >> 10710229

Jeune asphyxiating thoracic dystrophy and short-rib polydactyly type III (Verma-Naumoff) are variants of the same disorder.

N C Ho1, C A Francomano, M van Allen.   

Abstract

Jeune syndrome (JS) and short-rib polydactyly syndrome type III (SRP type III) are autosomal recessive disorders characterized by short ribs and polydactyly. They are distinguished from each other by the more severe radiological and histological bone findings as well as the occurrence of facial anomalies, ambiguous genitalia, and occasionally, cloacal abnormalities in SRP type III. We present a family in which two children have mild JS and one has SRP type III as evidence that JS and SRP type III are variants of the same disorder. The intrafamilial variability may reflect the effects of modifying loci on gene expression.

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Mesh:

Year:  2000        PMID: 10710229     DOI: 10.1002/(sici)1096-8628(20000214)90:4<310::aid-ajmg9>3.0.co;2-n

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


  15 in total

1.  Co-occurrence of Joubert syndrome and Jeune asphyxiating thoracic dystrophy.

Authors:  A M Lehman; P Eydoux; D Doherty; I A Glass; D Chitayat; B Y H Chung; S Langlois; S L Yong; R B Lowry; F Hildebrandt; P Trnka
Journal:  Am J Med Genet A       Date:  2010-06       Impact factor: 2.802

2.  Asphyxiating thoracic dystrophy with facial dysmorphism.

Authors:  V H Sankar; Shubha R Phadke
Journal:  Indian J Pediatr       Date:  2006-12       Impact factor: 1.967

3.  Ciliopathies with skeletal anomalies and renal insufficiency due to mutations in the IFT-A gene WDR19.

Authors:  Cecilie Bredrup; Sophie Saunier; Machteld M Oud; Torunn Fiskerstrand; Alexander Hoischen; Damien Brackman; Sabine M Leh; Marit Midtbø; Emilie Filhol; Christine Bole-Feysot; Patrick Nitschké; Christian Gilissen; Olav H Haugen; Jan-Stephan F Sanders; Irene Stolte-Dijkstra; Dorus A Mans; Eric J Steenbergen; Ben C J Hamel; Marie Matignon; Rolph Pfundt; Cécile Jeanpierre; Helge Boman; Eyvind Rødahl; Joris A Veltman; Per M Knappskog; Nine V A M Knoers; Ronald Roepman; Heleen H Arts
Journal:  Am J Hum Genet       Date:  2011-10-20       Impact factor: 11.025

Review 4.  Skeletal dysplasias.

Authors:  Deborah Krakow
Journal:  Clin Perinatol       Date:  2015-04-08       Impact factor: 3.430

5.  An Ift80 mouse model of short rib polydactyly syndromes shows defects in hedgehog signalling without loss or malformation of cilia.

Authors:  Suzanne Rix; Amelie Calmont; Peter J Scambler; Philip L Beales
Journal:  Hum Mol Genet       Date:  2011-01-12       Impact factor: 6.150

6.  DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III.

Authors:  Nathalie Dagoneau; Marie Goulet; David Geneviève; Yves Sznajer; Jelena Martinovic; Sarah Smithson; Céline Huber; Geneviève Baujat; Elisabeth Flori; Laura Tecco; Denise Cavalcanti; Anne-Lise Delezoide; Valérie Serre; Martine Le Merrer; Arnold Munnich; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2009-05       Impact factor: 11.025

7.  Short rib polydactyly syndrome-Type I.

Authors:  S Sridhar; Ravi Kishore; Niranjan Thomas; Atanu Kumar Jana
Journal:  Indian J Pediatr       Date:  2004-04       Impact factor: 1.967

8.  Mutations in the gene encoding IFT dynein complex component WDR34 cause Jeune asphyxiating thoracic dystrophy.

Authors:  Miriam Schmidts; Julia Vodopiutz; Sonia Christou-Savina; Claudio R Cortés; Aideen M McInerney-Leo; Richard D Emes; Heleen H Arts; Beyhan Tüysüz; Jason D'Silva; Paul J Leo; Tom C Giles; Machteld M Oud; Jessica A Harris; Marije Koopmans; Mhairi Marshall; Nursel Elçioglu; Alma Kuechler; Detlef Bockenhauer; Anthony T Moore; Louise C Wilson; Andreas R Janecke; Matthew E Hurles; Warren Emmet; Brooke Gardiner; Berthold Streubel; Belinda Dopita; Andreas Zankl; Hülya Kayserili; Peter J Scambler; Matthew A Brown; Philip L Beales; Carol Wicking; Emma L Duncan; Hannah M Mitchison
Journal:  Am J Hum Genet       Date:  2013-10-31       Impact factor: 11.025

9.  WDR34 mutations that cause short-rib polydactyly syndrome type III/severe asphyxiating thoracic dysplasia reveal a role for the NF-κB pathway in cilia.

Authors:  Céline Huber; Sulin Wu; Ashley S Kim; Sabine Sigaudy; Anna Sarukhanov; Valérie Serre; Genevieve Baujat; Kim-Hanh Le Quan Sang; David L Rimoin; Daniel H Cohn; Arnold Munnich; Deborah Krakow; Valérie Cormier-Daire
Journal:  Am J Hum Genet       Date:  2013-10-31       Impact factor: 11.025

10.  Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis.

Authors:  Pleasantine Mill; Paul J Lockhart; Elizabeth Fitzpatrick; Hayley S Mountford; Emma A Hall; Martin A M Reijns; Margaret Keighren; Melanie Bahlo; Catherine J Bromhead; Peter Budd; Salim Aftimos; Martin B Delatycki; Ravi Savarirayan; Ian J Jackson; David J Amor
Journal:  Am J Hum Genet       Date:  2011-04-08       Impact factor: 11.025

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