Neuropediatrics 2019; 50(S 02): S1-S55
DOI: 10.1055/s-0039-1698176
Oral Presentations
Neuromuscular Diseases and Varia
Georg Thieme Verlag KG Stuttgart · New York

Clinical Outcome of Children with Corpus Callosum Agenesis

Vera Raile
1   Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, SPZ Neuropädiatrie, Berlin, Germany
,
Nina Herz
1   Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, SPZ Neuropädiatrie, Berlin, Germany
,
Gabriel Promnitz
1   Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, SPZ Neuropädiatrie, Berlin, Germany
,
Joanna Schneider
1   Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, SPZ Neuropädiatrie, Berlin, Germany
,
Angela Maria Kaindl
1   Department of Pediatric Neurology, Charité - Universitätsmedizin Berlin, SPZ Neuropädiatrie, Berlin, Germany
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Publikationsverlauf

Publikationsdatum:
11. September 2019 (online)

 

Background: Agenesis of the corpus callosum (ACC) is a common cerebral malformation (prevalence approximately 1.8:10,000 live births). The range of CC malformations includes isolated agenesis (partial or complete) as well as hypoplasia. Additional cerebral malformations and extracerebral malformations may be associated; more than 200 genetic syndromes include an ACC. The diagnosis of an ACC is made predominantly prenatal. The development of children with isolated ACC is age-appropriate in approx. 75%. Nevertheless, evidence based prenatal counseling has been low so far.

Objective: Neurodevelopmental outcome in children with ACC to improve evidence based prenatal counseling.

Patients and Methods: Since 2010, a total of 23 children with ACC have been cared for in the Center for Chronically Sick Children, Charité. For 17 children, initial contact has already been carried out as part of our prenatal counseling. Pre- and postnatal imaging (ultrasound, fetal/postnatal cMRT), associated malformations, genetic and clinical findings, and psychological testing (Bayley, K-ABC, SONR, WPPSI) were included. The clinical outcome was classified as "normal" (IQ 85–115, unremarkable motor skills), "moderate developmental delay" (IQ 70–85, mild motor abnormalities), "severe developmental disorder" (IQ <70, severe movement disorder).

Results: Gender distribution was balanced; median age at last examination was 3.5 years (0.4–16.5 years). Isolated CC malformation was diagnosed in 15/23 (65%), associated CNS malformations in 4/23 (17%), and associated CNS malformations plus intracranial cyst in 4/23 (17%) children. Overall, a normal outcome showed 14/23 (61%) children, a moderate delay 5/23 (22%), and a severe developmental delay 4/23 (17%). All of the 4 severely affected children had an isolated ACC, three of them with syndromal genesis.

Conclusion: Children with ACC show a predominantly favourable outcome, nevertheless severe developmental disorders can occur. Associated CNS malformations are not necessarily associated with a worse outcome. Developmental disorders in ACC are more related to mental development than movement disorders. For evidence-based prenatal counseling of pregnant women, different subgroups must be consistently classified and prospective studies are needed.

References

1. D’Antonio F, Pagani G, Familiari A, et al. Outcomes associated with isolated agenesis of the corpus callosum: a meta-analysis. Pediatrics 2016;138(3):e20160445 10.1542/peds.2016-0445

2. D’Antonio F, Pagani G, Familiari A, et al. Outcomes associated with isolated agenesis of the corpus callosum: a meta-analysis. Pediatrics 2016;138(3):e20160445 10.1542/peds.2016-0445