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Research ArticlePediatrics

Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different Prognosis

C.A.P.F. Alves, J. Sidpra, A. Manteghinejad, S. Sudhakar, F.V. Massey, K.A. Aldinger, P. Haldipur, L.T. Lucato, S.F. Ferraciolli, S.R. Teixeira, Ö. Öztekin, D. Bhattacharya, A. Taranath, S.P. Prabhu, D.M. Mirsky, S. Andronikou, K.J. Millen, A.J. Barkovich, E. Boltshauser, W.B. Dobyns, M.J. Barkovich, M.T. Whitehead and K. Mankad
American Journal of Neuroradiology October 2023, 44 (10) 1201-1207; DOI: https://doi.org/10.3174/ajnr.A7967
C.A.P.F. Alves
aFrom the Division of Neuroradiology (C.A.P.F.A., A.M., S.R.T., S.A., M.T.W.), Department of Radiology, Children’s Hospital of Philadelphia, Philadephia, Pennsylvania
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J. Sidpra
bUnit of Neuroradiology (J.S., S.S., K.M.), Great Ormond Street Hospital for Children, National Health Service Foundation Trust, London, United Kingdom
cDevelopmental Biology & Cancer Section (J.S., K.M.), University College London Great Ormond Street Institute of Child Health, London, United Kingdom
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A. Manteghinejad
aFrom the Division of Neuroradiology (C.A.P.F.A., A.M., S.R.T., S.A., M.T.W.), Department of Radiology, Children’s Hospital of Philadelphia, Philadephia, Pennsylvania
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S. Sudhakar
bUnit of Neuroradiology (J.S., S.S., K.M.), Great Ormond Street Hospital for Children, National Health Service Foundation Trust, London, United Kingdom
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F.V. Massey
dUnit of Functional Neurosurgery (F.V.M.), National Hospital for Neurology & Neurosurgery, London, United Kingdom
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K.A. Aldinger
eCenter for Integrative Brain Research (K.A.A., P.H., K.J.M.), Seattle Children’s Research Institute, Seattle, Washington
fDepartments of Pediatrics and Neurology (K.A.A., P.H., K.J.M.), University of Washington, Seattle, Washington
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P. Haldipur
eCenter for Integrative Brain Research (K.A.A., P.H., K.J.M.), Seattle Children’s Research Institute, Seattle, Washington
fDepartments of Pediatrics and Neurology (K.A.A., P.H., K.J.M.), University of Washington, Seattle, Washington
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L.T. Lucato
gDepartment of Radiology, Division of Neuroradiology (L.T.L., S.F.F.), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil
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S.F. Ferraciolli
gDepartment of Radiology, Division of Neuroradiology (L.T.L., S.F.F.), Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil
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S.R. Teixeira
aFrom the Division of Neuroradiology (C.A.P.F.A., A.M., S.R.T., S.A., M.T.W.), Department of Radiology, Children’s Hospital of Philadelphia, Philadephia, Pennsylvania
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Ö. Öztekin
hDepartment of Neuroradiology (Ö.Ö.), Bakırçay University, Çiğli Education and Research Hospital, İzmir, Turkey
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D. Bhattacharya
iDepartment of Neuroradiology (D.B.), Royal Victoria Hospital, Belfast, UK
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A. Taranath
jDepartment of Medical Imaging (A.T.), Women's and Children’s Hospital, Adelaide, South Australia, Australia
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S.P. Prabhu
kDepartment of Radiology, Neuroradiology Division (S.P.P.), Boston Children’s Hospital, Boston, Massachusetts
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D.M. Mirsky
lDepartment of Radiology, Neuroradiology Division (D.M.M.), Children’s Hospital Colorado, Aurora, Colorado
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S. Andronikou
aFrom the Division of Neuroradiology (C.A.P.F.A., A.M., S.R.T., S.A., M.T.W.), Department of Radiology, Children’s Hospital of Philadelphia, Philadephia, Pennsylvania
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K.J. Millen
eCenter for Integrative Brain Research (K.A.A., P.H., K.J.M.), Seattle Children’s Research Institute, Seattle, Washington
fDepartments of Pediatrics and Neurology (K.A.A., P.H., K.J.M.), University of Washington, Seattle, Washington
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A.J. Barkovich
mDepartment of Neuroradiology (A.J.B., M.J.B.), University of California, San Francisco, San Francisco, California
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E. Boltshauser
nDepartment of Pediatric Neurology (E.B.), University Children’s Hospital, Zürich, Switzerland
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W.B. Dobyns
oDepartment of Genetics and Metabolism (W.B.D.), University of Minnesota, Minneaplis, Minnesota
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M.J. Barkovich
mDepartment of Neuroradiology (A.J.B., M.J.B.), University of California, San Francisco, San Francisco, California
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M.T. Whitehead
aFrom the Division of Neuroradiology (C.A.P.F.A., A.M., S.R.T., S.A., M.T.W.), Department of Radiology, Children’s Hospital of Philadelphia, Philadephia, Pennsylvania
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K. Mankad
bUnit of Neuroradiology (J.S., S.S., K.M.), Great Ormond Street Hospital for Children, National Health Service Foundation Trust, London, United Kingdom
cDevelopmental Biology & Cancer Section (J.S., K.M.), University College London Great Ormond Street Institute of Child Health, London, United Kingdom
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Abstract

BACKGROUND AND PURPOSE: Although cardinal imaging features for the diagnostic criteria of the Dandy-Walker phenotype have been recently defined, there is a large range of unreported malformations among these patients. The brainstem, in particular, deserves careful attention because malformations in this region have potentially important implications for clinical outcomes. In this article, we offer detailed information on the association of brainstem dysgenesis in a large, multicentric cohort of patients with the Dandy-Walker phenotype, defining different subtypes of involvement and their potential clinical impact.

MATERIALS AND METHODS: In this established multicenter cohort of 329 patients with the Dandy-Walker phenotype, we include and retrospectively review the MR imaging studies and clinical records of 73 subjects with additional brainstem malformations. Detailed evaluation of the different patterns of brainstem involvement and their potential clinical implications, along with comparisons between posterior fossa measurements for the diagnosis of the Dandy-Walker phenotype, was performed among the different subgroups of patients with brainstem involvement.

RESULTS: There were 2 major forms of brainstem involvement in patients with Dandy-Walker phenotype including the following: 1) the mild form with anteroposterior disproportions of the brainstem structures “only” (57/73; 78%), most frequently with pontine hypoplasia (44/57; 77%), and 2) the severe form with patients with tegmental dysplasia with folding, bumps, and/or clefts (16/73; 22%). Patients with severe forms of brainstem malformation had significantly increased rates of massive ventriculomegaly, additional malformations involving the corpus callosum and gray matter, and interhemispheric cysts. Clinically, patients with the severe form had significantly increased rates of bulbar dysfunction, seizures, and mortality.

CONCLUSIONS: Additional brainstem malformations in patients with the Dandy-Walker phenotype can be divided into 2 major subgroups: mild and severe. The severe form, though less prevalent, has characteristic imaging features, including tegmental folding, bumps, and clefts, and is directly associated with a more severe clinical presentation and increased mortality.

ABBREVIATION:

DW
Dandy-Walker phenotype
  • © 2023 by American Journal of Neuroradiology
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American Journal of Neuroradiology: 44 (10)
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Cite this article
C.A.P.F. Alves, J. Sidpra, A. Manteghinejad, S. Sudhakar, F.V. Massey, K.A. Aldinger, P. Haldipur, L.T. Lucato, S.F. Ferraciolli, S.R. Teixeira, Ö. Öztekin, D. Bhattacharya, A. Taranath, S.P. Prabhu, D.M. Mirsky, S. Andronikou, K.J. Millen, A.J. Barkovich, E. Boltshauser, W.B. Dobyns, M.J. Barkovich, M.T. Whitehead, K. Mankad
Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different Prognosis
American Journal of Neuroradiology Oct 2023, 44 (10) 1201-1207; DOI: 10.3174/ajnr.A7967

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Dandy-Walker Phenotype with Brainstem Involvement
C.A.P.F. Alves, J. Sidpra, A. Manteghinejad, S. Sudhakar, F.V. Massey, K.A. Aldinger, P. Haldipur, L.T. Lucato, S.F. Ferraciolli, S.R. Teixeira, Ö. Öztekin, D. Bhattacharya, A. Taranath, S.P. Prabhu, D.M. Mirsky, S. Andronikou, K.J. Millen, A.J. Barkovich, E. Boltshauser, W.B. Dobyns, M.J. Barkovich, M.T. Whitehead, K. Mankad
American Journal of Neuroradiology Oct 2023, 44 (10) 1201-1207; DOI: 10.3174/ajnr.A7967
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