Moyamoya syndrome in a child with methyl tetrahydrofolate reductase mutation

Neurol India. 2017 Nov-Dec;65(6):1408-1409. doi: 10.4103/0028-3886.217935.

Authors

Sanjeev K Bhoi¹, Suprava Naik², Deepanshu Dubey³, Jayantee Kalita³, Usha Kant Misra³

Affiliations

¹ Department of Neurology, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.
² Department of Radiodiagnosis, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India.
³ Department of Neurology, Sanjay Gandhi Postgraduate Institute of Medical Science, Lucknow, Uttar Pradesh, India.

PMID: 29133725
DOI: 10.4103/0028-3886.217935

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Brain / diagnostic imaging
Child
Humans
Magnetic Resonance Imaging
Male
Methylenetetrahydrofolate Reductase (NADPH2) / genetics*
Moyamoya Disease / diagnostic imaging
Moyamoya Disease / genetics*
Mutation

Substances

MTHFR protein, human
Methylenetetrahydrofolate Reductase (NADPH2)