Evidence map›Paper›PMID 41041388›Full record

ArticleCase reports in medicine2025

Dyke-Davidoff-Masson Syndrome in Pediatrics: Case Report of Atypical Status Epilepticus and Therapeutic Challenges in the Caribbean.

María Belén Martín-Sanz, Delvis Lucas-Muñoz, Manuel Colomé-Hidalgo, Gabriela Vásquez-Gómez

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Article in Case reports in medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

4 authors.

María Belén Martín-SanzDepartment of Medical Specialties and Public Health, Research Group of Humanities and Qualitative Research in Health Science, Rey Juan Carlos University, Alcorcón, Spain.ORCID https://orcid.org/0000-0001-8628-0979
Delvis Lucas-MuñozDepartment of Pediatric Neurology, Dr. Hugo Mendoza Pediatric Hospital, Santo Domingo, Dominican Republic.ORCID https://orcid.org/0009-0008-5662-7351
Manuel Colomé-HidalgoDepartment of Public Health, Autonomous University of Santo Domingo (UASD), Santo Domingo, Dominican Republic.ORCID https://orcid.org/0000-0002-4562-6491
Gabriela Vásquez-GómezDepartment of Pediatric Neurology, Dr. Hugo Mendoza Pediatric Hospital, Santo Domingo, Dominican Republic.ORCID https://orcid.org/0009-0001-8323-2207

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dyke-Davidoff-Masson syndrome (DDMS), also known as cerebral hemiatrophy, is characterized by brain damage resulting in hypoplasia of one cerebral hemisphere. It is described as a rare disorder, primarily characterized by epileptic seizures and convulsions, as well as hemiparesis and cognitive impairments. We present the evolution of a child with DDMS and the neurodevelopmental milestones achieved from the onset of symptoms at 10 days of age to 3 years. Clinical features included persistent seizures and hemiparesis. Neuroimaging revealed right cerebral hemiatrophy with associated structural changes. The aim of this study is to present a case report of a pediatric patient with DDMS, detailing the clinical evaluation, therapeutic approaches, and disease progression, while describing the healthcare process and challenges associated with managing this rare condition in the Dominican Republic. Through this, we aim to improve the therapeutic strategies implemented in the region for the management of this infrequent condition and enhance the understanding of DDMS in the Caribbean.

Indexed as

case reportcerebral hemiatrophyDyke–Davidoff–Masson syndrome (DDMS)status epilepticus

Identifiers

PMID41041388
PMCPMC12488304

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