Literature DB >> 7739837

Fetal akinesia.

E Hammond1, A E Donnenfeld.   

Abstract

Normal fetal growth and development during pregnancy is highly dependent upon adequate fetal movement. Limitation of movement, regardless of the underlying cause, can result in a particular pattern of abnormal fetal morphogenesis. This phenotype is termed the fetal akinesia deformation sequence (FADS). The etiology of fetal akinesia may be generally classified into one of five categories: neuropathy, myopathy, restrictive dermopathy, teratogen exposure, or restricted movement due to intrauterine constraint. In this article, the differential diagnosis of fetal akinesia is systematically reviewed and information regarding prenatal diagnosis, prognosis, perinatal management, and recurrence risks are discussed.

Entities:  

Mesh:

Year:  1995        PMID: 7739837     DOI: 10.1097/00006254-199503000-00028

Source DB:  PubMed          Journal:  Obstet Gynecol Surv        ISSN: 0029-7828            Impact factor:   2.347


  11 in total

1.  Escobar syndrome is a prenatal myasthenia caused by disruption of the acetylcholine receptor fetal gamma subunit.

Authors:  Katrin Hoffmann; Juliane S Muller; Sigmar Stricker; Andre Megarbane; Anna Rajab; Tom H Lindner; Monika Cohen; Eliane Chouery; Lynn Adaimy; Ismat Ghanem; Valerie Delague; Eugen Boltshauser; Beril Talim; Rita Horvath; Peter N Robinson; Hanns Lochmüller; Christoph Hübner; Stefan Mundlos
Journal:  Am J Hum Genet       Date:  2006-06-20       Impact factor: 11.025

2.  A Truncating Variant of CHRNG as a Cause of Escobar Syndrome: A Multiple Pterygium Syndrome Subtype.

Authors:  Alexander J Sandweiss; Shalinkumar Patel; Mohammad Y Bader; Ranjit I Kylat
Journal:  J Pediatr Genet       Date:  2020-08-26

Review 3.  Restrictive dermopathy--a lethal congenital laminopathy. Case report and review of the literature.

Authors:  Paulo Morais; Sofia Magina; Maria do Céu Ribeiro; Manuela Rodrigues; José Manuel Lopes; Huong Le Thi Thanh; Manfred Wehnert; Hercília Guimarães
Journal:  Eur J Pediatr       Date:  2008-11-20       Impact factor: 3.183

4.  Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders.

Authors:  Anne Michalk; Sigmar Stricker; Jutta Becker; Rosemarie Rupps; Tapio Pantzar; Jan Miertus; Giovanni Botta; Valeria G Naretto; Catrin Janetzki; Nausheen Yaqoob; Claus-Eric Ott; Dominik Seelow; Dagmar Wieczorek; Britta Fiebig; Brunhilde Wirth; Markus Hoopmann; Marisa Walther; Friederike Körber; Markus Blankenburg; Stefan Mundlos; Raoul Heller; Katrin Hoffmann
Journal:  Am J Hum Genet       Date:  2008-02       Impact factor: 11.025

Review 5.  Mechanobiology of embryonic skeletal development: Insights from animal models.

Authors:  Niamh C Nowlan; James Sharpe; Karen A Roddy; Patrick J Prendergast; Paula Murphy
Journal:  Birth Defects Res C Embryo Today       Date:  2010-09

6.  Diagnosing arthrogryposis multiplex congenita: a review.

Authors:  Emmanouil Kalampokas; Theodoros Kalampokas; Chrisostomos Sofoudis; Efthymios Deligeoroglou; Dimitrios Botsis
Journal:  ISRN Obstet Gynecol       Date:  2012-09-23

7.  Mechanical influences on morphogenesis of the knee joint revealed through morphological, molecular and computational analysis of immobilised embryos.

Authors:  Karen A Roddy; Patrick J Prendergast; Paula Murphy
Journal:  PLoS One       Date:  2011-02-28       Impact factor: 3.240

8.  Biophysical stimuli induced by passive movements compensate for lack of skeletal muscle during embryonic skeletogenesis.

Authors:  Niamh C Nowlan; Gerard Dumas; Shahragim Tajbakhsh; Patrick J Prendergast; Paula Murphy
Journal:  Biomech Model Mechanobiol       Date:  2011-04-20

9.  Arthrogryposis: an update on clinical aspects, etiology, and treatment strategies.

Authors:  Bartłomiej Kowalczyk; Jarosław Feluś
Journal:  Arch Med Sci       Date:  2016-02-02       Impact factor: 3.318

Review 10.  Pena-Shokeir syndrome: current management strategies and palliative care.

Authors:  Sumaiya Adam; Melantha Coetzee; Engela Magdalena Honey
Journal:  Appl Clin Genet       Date:  2018-10-25
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.