JOURNAL
Clinical case of a patient with Dyke-Davidoff-Masson syndrome
About the Authors
Aidana Aubakir – Senior neurologist of the psychoneurological department No. 5 "Balbulak", NJSC "National Center for Children's Rehabilitation", Astana, Kazakhstan, This email address is being protected from spambots. You need JavaScript enabled to view it., ORCID: 0009-0007-9151-8823
Zhadyra Kurmanova – Head of the psychoneurological department No. 4 "Akzhol", NJSC "National Center for Children's Rehabilitation", Astana, Kazakhstan, This email address is being protected from spambots. You need JavaScript enabled to view it., ORCID: 0009-0007-8367-2070
Аbstract
Dyke-Davidoff-Masson syndrome (DDMS) is a rare pathology that refers to atrophy or hypoplasia of one hemisphere of the brain (hemiatrophy), which usually occurs due to a stroke of the developing brain in the fetal or early childhood period. About 10 cases of this syndrome have been described in the world, which classifies it as a rare pathology of the brain. A 7-year-old girl was admitted to our Center for a rehabilitation course under the guise of a diagnosis of "Cerebral palsy", but with symptoms of this rare syndrome, with confirming radiological criteria. We decided to describe this clinical case in detail with an analysis of Dyke-Davidoff-Masson syndrome.
Keywords
Dyke-Davidoff-Masson syndrome, cerebral palsy, hemiatrophy, epilepsy, DDMS syndrome
References
- Dyke C.G., Davidoff L.M., Masson C.B. (1933). Cerebral hemiatrophy and homolateral hypertrophy of the skull and sinuses. Surg Gynecol Obstet. 57, 588–600.
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- Atalar M.H., Icagasioglu D., Tas F. (2013). Dyke–Davidoff–Masson syndrome: clinical and radiological characteristics of typical and atypical cases. Acta Neurol Belg., 113(2), 111–119.
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