Literature DB >> 22430728

Isolated corpus callosum agenesis: a ten-year follow-up after prenatal diagnosis (how are the children without corpus callosum at 10 years of age?).

Marie-Laure Moutard1, Virginie Kieffer, Josué Feingold, Fanny Lewin, Jean-Michel Baron, Catherine Adamsbaum, Antoinette Gélot, Arnaud Isapof, François Kieffer, Thierry Billette de Villemeur.   

Abstract

BACKGROUND: Corpus callosum agenesis (CCA) is generally diagnosed in utero. Outcome appears to be better if the malformation is isolated. The aim of this study, which is the first one with a long (10 years) and standardized follow up, was to report cognitive abilities of children with isolated CCA diagnosed prenatally.
METHODS: We prospectively evaluated 17 children. Clinical examinations, neuropsychological tests were performed each year. School achievement and personal and familial data were collected.
RESULTS: Twelve children completed the entire follow up. One child was finally considered to have associated CCA, because signs of fetal alcohol syndrome had become obvious. Of the 11 other children, three (27%) had borderline intelligence whereas the intelligence levels of eight (73%) were in the normal range, although half of these children experienced some difficulties in scholastic achievement. Neither epilepsy nor intellectual deficiency was noted and intellectual quotient scores correlated strongly with the mother's education level.
CONCLUSION: Although prenatal diagnosis of isolated CCA is reliable, false postnatal diagnoses remain possible (10-20%) even with complete prenatal screening. Outcome is mostly favorable because intelligence is within the normal range for nearly 3/4 of the children. However, they frequently have mild learning difficulties.
© 2012 John Wiley & Sons, Ltd.

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Mesh:

Year:  2012        PMID: 22430728     DOI: 10.1002/pd.3824

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  10 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.  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

3.  Corpus callosum measurements correlate with developmental delay in Smith-Lemli-Opitz syndrome.

Authors:  Ryan W Y Lee; Shoko Yoshida; Eun Sol Jung; Susumu Mori; Eva H Baker; Forbes D Porter
Journal:  Pediatr Neurol       Date:  2013-08       Impact factor: 3.372

4.  Complete corpus callosum agenesis: can it be mild?

Authors:  Matteo Chiappedi; Anna Fresca; Ilaria Maria Carlotta Baschenis
Journal:  Case Rep Pediatr       Date:  2012-08-29

5.  Clinical outcomes and neurodevelopmental outcome of prenatally diagnosed agenesis of corpus callosum in single center of Korea.

Authors:  Sung Eun Kim; Hye-In Jang; Kylie Hae-Jin Chang; Ji-Hee Sung; Jiwon Lee; Jeehun Lee; Suk-Joo Choi; Soo-Young Oh; Cheong-Rae Roh; Jong-Hwa Kim
Journal:  Obstet Gynecol Sci       Date:  2017-01-15

6.  Analyses of pathological cranial ultrasound findings in neonates that fall outside recent indication guidelines: results of a population-based birth cohort: survey of neonates in Pommerania (SNiP-study).

Authors:  Judith Weise; Matthias Heckmann; Hagen Bahlmann; Till Ittermann; Heike Allenberg; Grzegorz Domanski; Anja Erika Lange
Journal:  BMC Pediatr       Date:  2019-12-05       Impact factor: 2.125

7.  Effect of corpus callosum agenesis on the language network in children and adolescents.

Authors:  Lisa Bartha-Doering; Ernst Schwartz; Kathrin Kollndorfer; Florian Ph S Fischmeister; Astrid Novak; Georg Langs; Harald Werneck; Daniela Prayer; Rainer Seidl; Gregor Kasprian
Journal:  Brain Struct Funct       Date:  2021-01-26       Impact factor: 3.270

8.  Long-term follow-up in a cohort of children with isolated corpus callosum agenesis at fetal MRI.

Authors:  Romina Romaniello; Filippo Arrigoni; Patrizia De Salvo; Maria Clara Bonaglia; Elena Panzeri; Maria Teresa Bassi; Cecilia Parazzini; Andrea Righini; Renato Borgatti
Journal:  Ann Clin Transl Neurol       Date:  2021-12-01       Impact factor: 4.511

9.  Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation.

Authors:  Boris Keren; Delphine Héron; Solveig Heide; Myrtille Spentchian; Stéphanie Valence; Julien Buratti; Corinne Mach; Elodie Lejeune; Valérie Olin; Marta Massimello; Daphné Lehalle; Linda Mouthon; Sandra Whalen; Anne Faudet; Cyril Mignot; Catherine Garel; Eleonore Blondiaux; Mathilde Lefebvre; Geneviève Quenum-Miraillet; Sandra Chantot-Bastaraud; Mathieu Milh; Florence Bretelle; Vincent des Portes; Laurent Guibaud; Audrey Putoux; Vassili Tsatsaris; Marta Spodenkiewic; Valérie Layet; Rodolphe Dard; Laurent Mandelbrot; Agnès Guet; Sébastien Moutton; Magali Gorce; Mathilde Nizon; Marie Vincent; Claire Beneteau; Marie-Amélie Rocchisanni; Alexandra Benachi; Julien Saada; Tania Attié-Bitach; Lucie Guilbaud; Paul Maurice; Stéphanie Friszer; Jean-Marie Jouannic; Thierry Billette de Villemeur; Marie-Laure Moutard
Journal:  Genet Med       Date:  2020-06-22       Impact factor: 8.822

10.  Isolated agenesis of the corpus callosum and normal general intelligence development during postnatal life: a case report and review of the literature.

Authors:  Parménides Guadarrama-Ortiz; José Alberto Choreño-Parra; Tania de la Rosa-Arredondo
Journal:  J Med Case Rep       Date:  2020-02-12
  10 in total

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