DYKE DAVIDOFF MASSON SYNDROME IN A FUNCTIONALLY INDEPENDENT ADULT WITH CHILDHOOD ONSET HEMIPARESIS: A CASE REPORT

Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological disorder characterized by cerebral hemiatrophy, contralateral hemiparesis, facial asymmetry, and recurrent seizures. It typically presents during childhood, while diagnosis in adulthood is uncommon, particularly in individuals who remain functionally independent. We report the case of a 37-year-old male with childhood-onset hemiparesis who remained ambulatory and independent in activities of daily living. The diagnosis of DDMS was established incidentally on magnetic resonance imaging (MRI) during evaluation for an unrelated illness. This case highlights the variable clinical spectrum of DDMS and emphasizes that mild cases may remain undiagnosed until adulthood.

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Publication Details

Journal
European Journal Pharmaceutical and Medical Research
Published
2026-10-01
DOI
https://doi.org/10.5281/zenodo.23032281
Primary Topic
Glycogen Storage Diseases and Myoclonus
Type
article
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article

DYKE DAVIDOFF MASSON SYNDROME IN A FUNCTIONALLY INDEPENDENT ADULT WITH CHILDHOOD ONSET HEMIPARESIS: A CASE REPORT

Dr. Hruthik Kumar T.1*, Dr. Alekya Katti2, Dr. Sai Kaushik Rathod3
European Journal Pharmaceutical and Medical Research
Glycogen Storage Diseases and Myoclonus
article

DYKE DAVIDOFF MASSON SYNDROME IN A FUNCTIONALLY INDEPENDENT ADULT WITH CHILDHOOD ONSET HEMIPARESIS: A CASE REPORT

Dr. Hruthik Kumar T.1*, Dr. Alekya Katti2, Dr. Sai Kaushik Rathod3
article en

Abstract

Dyke-Davidoff-Masson syndrome (DDMS) is a rare neurological disorder characterized by cerebral hemiatrophy, contralateral hemiparesis, facial asymmetry, and recurrent seizures. It typically presents during childhood, while diagnosis in adulthood is uncommon, particularly in individuals who remain functionally independent. We report the case of a 37-year-old male with childhood-onset hemiparesis who remained ambulatory and independent in activities of daily living. The diagnosis of DDMS was established incidentally on magnetic resonance imaging (MRI) during evaluation for an unrelated illness. This case highlights the variable clinical spectrum of DDMS and emphasizes that mild cases may remain undiagnosed until adulthood.

European Journal Pharmaceutical and Medical Research
Good health and well-being
Openalex Percentile: Top 11%
Glycogen Storage Diseases and Myoclonus
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