Evidence map›Paper›PMID 37591769›Full record

ArticleAJNR. American journal of neuroradiology2023

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 and 13 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in AJNR. American journal of neuroradiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
3.5field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 13 institutions in 6 countries.

C A P F AlvesFrom 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 alvesc@chop.edu.ORCID 0000-0001-5877-9086
J SidpraUnit of Neuroradiology (J.S., S.S., K.M.), Great Ormond Street Hospital for Children, National Health Service Foundation Trust, London, United Kingdom.ORCID 0000-0003-1985-5503
A ManteghinejadFrom 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.ORCID 0000-0002-3847-5496
S SudhakarUnit of Neuroradiology (J.S., S.S., K.M.), Great Ormond Street Hospital for Children, National Health Service Foundation Trust, London, United Kingdom.ORCID 0000-0002-7632-9705
F V MasseyUnit of Functional Neurosurgery (F.V.M.), National Hospital for Neurology & Neurosurgery, London, United Kingdom.ORCID 0000-0002-8971-5680
K A AldingerCenter for Integrative Brain Research (K.A.A., P.H., K.J.M.), Seattle Children's Research Institute, Seattle, Washington.ORCID 0000-0002-5406-8911
P HaldipurCenter for Integrative Brain Research (K.A.A., P.H., K.J.M.), Seattle Children's Research Institute, Seattle, Washington.ORCID 0000-0003-2865-8683
L T LucatoDepartment 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.ORCID 0000-0001-9181-5245
S F FerraciolliDepartment 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.ORCID 0000-0001-5687-4186
S R TeixeiraFrom 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.ORCID 0000-0001-5845-058X
Ö ÖztekinDepartment of Neuroradiology (Ö.Ö.), Bakırçay University, Çiğli Education and Research Hospital, İzmir, Turkey.ORCID 0000-0002-0092-5260
D BhattacharyaDepartment of Neuroradiology (D.B.), Royal Victoria Hospital, Belfast, UK.ORCID 0000-0001-6679-012X
A TaranathDepartment of Medical Imaging (A.T.), Women's and Children's Hospital, Adelaide, South Australia, Australia.ORCID 0000-0002-2910-2436
S P PrabhuDepartment of Radiology, Neuroradiology Division (S.P.P.), Boston Children's Hospital, Boston, Massachusetts.ORCID 0000-0003-0871-115X
D M MirskyDepartment of Radiology, Neuroradiology Division (D.M.M.), Children's Hospital Colorado, Aurora, Colorado.ORCID 0000-0003-2162-515X
S AndronikouFrom 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.ORCID 0000-0002-1015-9790
K J MillenCenter for Integrative Brain Research (K.A.A., P.H., K.J.M.), Seattle Children's Research Institute, Seattle, Washington.ORCID 0000-0001-9978-675X
A J BarkovichDepartment of Neuroradiology (A.J.B., M.J.B.), University of California, San Francisco, San Francisco, California.ORCID 0000-0003-4291-7346
E BoltshauserDepartment of Pediatric Neurology (E.B.), University Children's Hospital, Zürich, Switzerland.ORCID 0000-0002-0791-2905
W B DobynsDepartment of Genetics and Metabolism (W.B.D.), University of Minnesota, Minneaplis, Minnesota.ORCID 0000-0002-7681-2844
M J BarkovichDepartment of Neuroradiology (A.J.B., M.J.B.), University of California, San Francisco, San Francisco, California.ORCID 0000-0002-8257-423X
M T WhiteheadFrom 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.ORCID 0000-0001-5077-693X
K MankadUnit of Neuroradiology (J.S., S.S., K.M.), Great Ormond Street Hospital for Children, National Health Service Foundation Trust, London, United Kingdom.ORCID 0000-0001-5979-9337
Children's Hospital of Philadelphia · USNational Health Service · GBUniversity of Washington · USHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversity of California, San Francisco · USBoston Children's Hospital · USChildren's Hospital Colorado · USIzmir University · TRNational Hospital for Neurology and Neurosurgery · GBUniversity Children's Hospital Zurich · CHUniversity of Minnesota · USUniversity of Ulster · GBWomen's and Children's Hospital · AU

Funding

Pathological Mechanisms of Human Cerebellar MalformationsR37NS095733 · NINDS · SEATTLE CHILDREN'S HOSPITAL · PI Kathleen Joyce Millen · 2021 to 2026
$5.5M
NINDS NIH HHS R37 NS095733
6 · The paper itself

Abstract

background and purposeAlthough 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

methodsIn 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.

resultsThere 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.

conclusionsAdditional 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.

Indexed as

Dandy-Walker SyndromeHydrocephalusNervous System MalformationsBrain StemHumansPrognosisRetrospective Studies

Identifiers

PMID37591769
PMCPMC10549954
OpenAlexW4385932798

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