Dyke-Davidoff-Masson Syndrome with crossed cerebellar atrophy

Authors

DOI:

https://doi.org/10.3126/njn.v18i3.37163

Keywords:

Cerebellar atrophy, Dyke-Davidoff-Masson syndrome, MRI

Abstract

Dyke-Davidoff-Masson Syndrome (DDMS) is a rare neurological condition characterised clinically by recurrent seizures, facial asymmetry, hemiplegia and mental retardation likely due to foetal or early childhood cerebral insult. We describe the MRI findings of DDMS in a 10-year-old male child. MRI brain revealed right cerebral atrophy, ipsilateral thickening of calvarium, right lateral ventricular dilatation, hyper-pneumatisation of frontal sinus, and contralateral cerebellar atrophy which are consistent with DDMS.

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Author Biographies

Rohit Kumar, Department of Radio-diagnosis, Indira Gandhi Institute of Medical Science, Patna, India

DNB, Junior Resident

Deepak Kumar, Department of Radio-diagnosis, Indira Gandhi Institute of Medical Science, Patna, India

Associate Professor

Himanshu Mishra, Department of Radio-diagnosis, Indira Gandhi Institute of Medical Science, Patna, India

DNB, Junior Resident

Sanjay Kumar Suman, Department of Radio-diagnosis, Indira Gandhi Institute of Medical Science, Patna, India

MD - Radiology

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Published

2021-09-01

How to Cite

1.
Kumar R, Kumar D, Mishra H, Suman SK, Prasad U. Dyke-Davidoff-Masson Syndrome with crossed cerebellar atrophy. Nep J Neurosci [Internet]. 2021 Sep. 1 [cited 2024 Dec. 26];18(3):73-5. Available from: https://nepjol.info./index.php/NJN/article/view/37163

Issue

Vol. 18 No. 3 (2021)

Section

Neuro View Box

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Copyright (c) 2021 Nepalese Society of Neurosurgeons (NESON)

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