Literature DB >> 16461029

Human laterality disorders.

Hilde Peeters1, Koen Devriendt.   

Abstract

Heterotaxia is a group of congenital disorders characterized by a misplacement of one or more organs according to the left-right axis. Bilateral asymmetry of internal organs is conserved among all vertebrate species. Analyses in animal models such as mouse, chicken, frog and zebrafish allowed for a remarkable progress of knowledge on the embryonic and genetic mechanisms underlying internal left-right asymmetry. In this review we focus on the insights from these model organisms that are useful for a better understanding of the etiology and pathogenesis of human heterotaxia. The known causes of human heterotaxia are reviewed and situated within the conceptual framework that originates from vertebrate model organisms. Furthermore, we attempt to apply the rapidly increasing insights gained from both animal models and human genetics to clinical practice in order to contribute to a more accurate conceptual classification, genetic diagnosis and counseling.

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Year:  2006        PMID: 16461029     DOI: 10.1016/j.ejmg.2005.12.003

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN: 1769-7212            Impact factor:   2.708


  54 in total

1.  Situs ambiguous in a schoolchild.

Authors:  Miguel Tortajada; Miriam Moreno; Miguel Gracia; Amparo Sanchis
Journal:  BMJ Case Rep       Date:  2009-11-26

2.  BCL6 canalizes Notch-dependent transcription, excluding Mastermind-like1 from selected target genes during left-right patterning.

Authors:  Daisuke Sakano; Akiko Kato; Nisarg Parikh; Kelly McKnight; Doris Terry; Branko Stefanovic; Yoichi Kato
Journal:  Dev Cell       Date:  2010-03-16       Impact factor: 12.270

3.  The ATP-sensitive K(+)-channel (K(ATP)) controls early left-right patterning in Xenopus and chick embryos.

Authors:  Sherry Aw; Joseph C Koster; Wade Pearson; Colin G Nichols; Nian-Qing Shi; Katia Carneiro; Michael Levin
Journal:  Dev Biol       Date:  2010-07-17       Impact factor: 3.582

4.  Consistent left-right asymmetry cannot be established by late organizers in Xenopus unless the late organizer is a conjoined twin.

Authors:  Laura N Vandenberg; Michael Levin
Journal:  Development       Date:  2010-04       Impact factor: 6.868

Review 5.  Follow your gut: relaying information from the site of left-right symmetry breaking in the mouse.

Authors:  Yukio Saijoh; Manuel Viotti; Anna-Katerina Hadjantonakis
Journal:  Genesis       Date:  2014-05-05       Impact factor: 2.487

6.  Early, nonciliary role for microtubule proteins in left-right patterning is conserved across kingdoms.

Authors:  Maria Lobikin; Gang Wang; Jingsong Xu; Yi-Wen Hsieh; Chiou-Fen Chuang; Joan M Lemire; Michael Levin
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-16       Impact factor: 11.205

Review 7.  A unified model for left-right asymmetry? Comparison and synthesis of molecular models of embryonic laterality.

Authors:  Laura N Vandenberg; Michael Levin
Journal:  Dev Biol       Date:  2013-04-10       Impact factor: 3.582

8.  LRRC50, a conserved ciliary protein implicated in polycystic kidney disease.

Authors:  Ellen van Rooijen; Rachel H Giles; Emile E Voest; Carina van Rooijen; Stefan Schulte-Merker; Freek J van Eeden
Journal:  J Am Soc Nephrol       Date:  2008-04-02       Impact factor: 10.121

9.  Laterality disturbance and hypopituitarism. A case report of co-existing situs inversus totalis and combined pituitary hormone deficiency.

Authors:  Z Halász; R Bertalan; J Toke; A Patócs; M Tóth; G Fekete; E Gláz; K Rácz
Journal:  J Endocrinol Invest       Date:  2008-01       Impact factor: 4.256

10.  Left-right asymmetry in the chick embryo requires core planar cell polarity protein Vangl2.

Authors:  Ying Zhang; Michael Levin
Journal:  Genesis       Date:  2009-11       Impact factor: 2.487

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