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. 2021 Sep-Oct;24(5):781-783.
doi: 10.4103/aian.AIAN_1130_20. Epub 2021 Feb 4.

CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders

Prateek K Panda  1 , Radhapyari Lourembam  1 , Indar K Sharawat  1
Affiliations

CNNM2 Heterozygous Variant Presenting as Hypomagnesemia and West Syndrome: Expanding the Spectrum of CNNM2 Gene-Related Epileptic Disorders

Prateek K Panda et al. Ann Indian Acad Neurol. 2021 Sep-Oct.
No abstract available

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Conflict of interest statement

There are no conflicts of interest.

Figures

Figure 1
Figure 1
A sedated electroencephalogram at 4-months of age (international 10-20 system, average montage, sensitivity: 7μV/mm, sweep speed: 30 mm/sec, low filter: 1 Hz and high filter 70 Hz) showing disorganized, asynchronous, chaotic high amplitude slow waves activity with interspersed multifocal spikes suggestive of Hypsarrhythmia
Figure 2
Figure 2
A sedated electroencephalogram at 16-months of age (international 10-20 system, bipolar montage, sensitivity: 7.5μV/mm, sweep speed: 30 mm/sec, low filter: 1 Hz and high filter 70 Hz) showing asymmetric and asynchronous generalized (frontal dominant), high amplitude spike-slow wave complexes with frequent polyspikes
See this image and copyright information in PMC

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