Literature DB >> 22284958

Neurodevelopment after prenatal diagnosis of isolated agenesis of the corpus callosum: an integrative review.

Alexandros Sotiriadis1, George Makrydimas.   

Abstract

OBJECTIVE: To systematically review published data on the neurodevelopment of children that were diagnosed prenatally with isolated agenesis of the corpus callosum. STUDY
DESIGN: Medline and Scopus searches (1960-July 2011); cross-referencing of retrieved articles.
RESULTS: Sixteen reports (132 cases of apparently isolated agenesis of the corpus callosum) were included in the analysis. The rates of normal outcome, borderline or moderate disability and severe disability were 94/132 (71.2%; 95% confidence interval [CI], 63.0-78.3), 18/132 (13.6%; 95% CI, 8.8-20.5), and 22/132 (15.2%; 95% CI, 10.0-22.2), respectively. Magnetic resonance imaging detected additional cerebral abnormalities in 22.5% (95% CI, 12.3-37.5) of apparently isolated agenesis of the corpus callosum cases. In truly isolated agenesis of the corpus callosum (confirmed by magnetic resonance imaging), the rates of normal neurodevelopment and severe disability were 52/69 (75.4%; 95% CI, 64.0-84.0) and 8/69 (11.6%; 95% CI, 6.0-21.2), respectively.
CONCLUSION: Prenatally diagnosed, isolated agenesis of the corpus callosum is usually associated with a favorable outcome. Larger, prospective series are required, as current data are limited, inconsistent, and prevent subgroup analyses (eg, complete vs partial agenesis of the corpus callosum).
Copyright © 2012 Mosby, Inc. All rights reserved.

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Year:  2011        PMID: 22284958     DOI: 10.1016/j.ajog.2011.12.024

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN: 0002-9378            Impact factor:   8.661


  22 in total

1.  Variability of Forebrain Commissures in Callosal Agenesis: A Prenatal MR Imaging Study.

Authors:  C Cesaretti; M Nanni; T Ghi; C Parazzini; G Conte; E Contro; G Grisolia; A Righini
Journal:  AJNR Am J Neuroradiol       Date:  2015-10-29       Impact factor: 3.825

2.  Malformations of Cerebral Cortex Development: Molecules and Mechanisms.

Authors:  Gordana Juric-Sekhar; Robert F Hevner
Journal:  Annu Rev Pathol       Date:  2019-01-24       Impact factor: 23.472

Review 3.  Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.

Authors:  Timothy J Edwards; Elliott H Sherr; A James Barkovich; Linda J Richards
Journal:  Brain       Date:  2014-01-28       Impact factor: 13.501

4.  Reply: ARID1B mutations are the major genetic cause of corpus callosum anomalies in patients with intellectual disability.

Authors:  Timothy J Edwards; Elliott H Sherr; A James Barkovich; Linda J Richards
Journal:  Brain       Date:  2016-11-01       Impact factor: 13.501

5.  Antenatal diagnosis and outcome of agenesis of corpus callosum: A retrospective review of 33 cases.

Authors:  Ozgür Ozyüncü; Aslıhan Yazıcıoğlu; Mert Turğal
Journal:  J Turk Ger Gynecol Assoc       Date:  2014-03-01

6.  Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance.

Authors:  Ashley P L Marsh; Delphine Heron; Timothy J Edwards; Angélique Quartier; Charles Galea; Caroline Nava; Agnès Rastetter; Marie-Laure Moutard; Vicki Anderson; Pierre Bitoun; Jens Bunt; Anne Faudet; Catherine Garel; Greta Gillies; Ilan Gobius; Justine Guegan; Solveig Heide; Boris Keren; Fabien Lesne; Vesna Lukic; Simone A Mandelstam; George McGillivray; Alissandra McIlroy; Aurélie Méneret; Cyril Mignot; Laura R Morcom; Sylvie Odent; Annalisa Paolino; Kate Pope; Florence Riant; Gail A Robinson; Megan Spencer-Smith; Myriam Srour; Sarah E M Stephenson; Rick Tankard; Oriane Trouillard; Quentin Welniarz; Amanda Wood; Alexis Brice; Guy Rouleau; Tania Attié-Bitach; Martin B Delatycki; Jean-Louis Mandel; David J Amor; Emmanuel Roze; Amélie Piton; Melanie Bahlo; Thierry Billette de Villemeur; Elliott H Sherr; Richard J Leventer; Linda J Richards; Paul J Lockhart; Christel Depienne
Journal:  Nat Genet       Date:  2017-02-27       Impact factor: 38.330

7.  Exome sequencing identifies recessive CDK5RAP2 variants in patients with isolated agenesis of corpus callosum.

Authors:  Loubna Jouan; Bouchra Ouled Amar Bencheikh; Hussein Daoud; Alexandre Dionne-Laporte; Sylvia Dobrzeniecka; Dan Spiegelman; Daniel Rochefort; Pascale Hince; Anna Szuto; Maryse Lassonde; Marine Barbelanne; William Y Tsang; Patrick A Dion; Hugo Théoret; Guy A Rouleau
Journal:  Eur J Hum Genet       Date:  2015-07-22       Impact factor: 4.246

8.  Structural connectivity analysis reveals abnormal brain connections in agenesis of the corpus callosum in children.

Authors:  Avner Meoded; Rohan Katipally; Thangamadhan Bosemani; Thierry A G M Huisman; Andrea Poretti
Journal:  Eur Radiol       Date:  2014-12-06       Impact factor: 5.315

9.  Agenesis of the corpus callosum. An autopsy study in fetuses.

Authors:  Debora Kidron; Daniel Shapira; Liat Ben Sira; Gustavo Malinger; Dorit Lev; Andreea Cioca; Reuven Sharony; Tally Lerman Sagie
Journal:  Virchows Arch       Date:  2015-11-16       Impact factor: 4.064

Review 10.  DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.

Authors:  Ashley P L Marsh; Timothy J Edwards; Charles Galea; Helen M Cooper; Elizabeth C Engle; Saumya S Jamuar; Aurélie Méneret; Marie-Laure Moutard; Caroline Nava; Agnès Rastetter; Gail Robinson; Guy Rouleau; Emmanuel Roze; Megan Spencer-Smith; Oriane Trouillard; Thierry Billette de Villemeur; Christopher A Walsh; Timothy W Yu; Delphine Heron; Elliott H Sherr; Linda J Richards; Christel Depienne; Richard J Leventer; Paul J Lockhart
Journal:  Hum Mutat       Date:  2017-11-11       Impact factor: 4.878

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