2016
DOI: 10.4103/1817-1745.193365
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Dyke–Davidoff–Masson syndrome: A rare cause of cerebral hemiatrophy in children

Abstract: Dyke–Davidoff–Masson syndrome (DDMS) is an uncommon condition, in which the diagnosis is mainly done by various clinical presentations along with positive radiological findings. Patients have facial asymmetry, seizures, learning difficulties, and contralateral hemiparesis. The radiological discoveries of the same incorporate cerebral hemiatrophy with homolateral hypertrophy of the skull and sinuses. Here, we report a case of a 10-year-old female child who presented with a single episode of convulsion, mental r… Show more

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Cited by 18 publications
(17 citation statements)
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“…Therefore, the patterns of brain atrophy may reflect the nature of the brain injury determinants. Hemi-atrophy seems to be rare according to this study and likewise in the overall global statistics [ 35 ]. The reason for this could be explained by the high possibility that the determinants of brain hemi-atrophy are more responsible for the condition during intra-uterine life than post natal life [ 36 ].…”
Section: Discussionmentioning
confidence: 56%
“…Therefore, the patterns of brain atrophy may reflect the nature of the brain injury determinants. Hemi-atrophy seems to be rare according to this study and likewise in the overall global statistics [ 35 ]. The reason for this could be explained by the high possibility that the determinants of brain hemi-atrophy are more responsible for the condition during intra-uterine life than post natal life [ 36 ].…”
Section: Discussionmentioning
confidence: 56%
“…[ 6 7 8 ] The differential diagnoses are Sturge–Weber syndrome, basal ganglia germinoma, Fishman syndrome, Silver–Russell syndrome, linear nevus syndrome, and Rasmussen's encephalitis, which have unique clinical and radiological features. [ 9 10 ]…”
Section: Discussionmentioning
confidence: 99%
“…It is associated with compensatory calvarium thickening, hyperpneumatization of the paranasal sinuses and mastoid cells, and elevation of the petrous ridge. [9] In congenital hemiatrophy, when the insult occurs in utero, there is a shift of midline structures toward the disease side, but there is the absence of sulcal prominence replacing the gliotic tissue. This is the salient feature differentiating congenital from acquired form.…”
Section: Discussionmentioning
confidence: 99%