Advanced search
Publication Cover
Neuropsychiatric Disease and Treatment Volume 10, 2014 - Issue
Submit an article Journal homepage
68
Views
4
CrossRef citations to date
0
Altmetric
Case Report

Spinal cord demyelination combined with hyperhomocysteinemia: a case report

Meimei HaoDepartment of Neurology, Xijing Hospital, Fourth Military Medical University, Xi’an, People’s Republic of China
,
Yan ZhangDepartment of Neurology, Xijing Hospital, Fourth Military Medical University, Xi’an, People’s Republic of China
,
Shuangxing HouDepartment of Neurology, Xijing Hospital, Fourth Military Medical University, Xi’an, People’s Republic of China
,
Yanling ChenDepartment of Neurology, Xijing Hospital, Fourth Military Medical University, Xi’an, People’s Republic of China
,
Ming ShiDepartment of Neurology, Xijing Hospital, Fourth Military Medical University, Xi’an, People’s Republic of China
,
Gang ZhaoDepartment of Neurology, Xijing Hospital, Fourth Military Medical University, Xi’an, People’s Republic of China
&
Yanchun DengDepartment of Neurology, Xijing Hospital, Fourth Military Medical University, Xi’an, People’s Republic of ChinaCorrespondence[email protected]
 show all
Pages 2057-2059 | Published online: 03 Nov 2014

Figures & data

Figure 1 (A) T2-weighted sagittal magnetic resonance image of the cervical and thoracic spinal cord without contrast medium showing a hyperintense lesion with swelling at C7 to T3 (arrow). (B) A follow-up spinal magnetic resonance image 3 months later showed almost complete disappearance of the original lesions.

Figure 1 (A) T2-weighted sagittal magnetic resonance image of the cervical and thoracic spinal cord without contrast medium showing a hyperintense lesion with swelling at C7 to T3 (arrow). (B) A follow-up spinal magnetic resonance image 3 months later showed almost complete disappearance of the original lesions.

Figure 2 The patient has a homozygous MTHFR gene mutation c.677C>T (p.A222V).

Note: The position is indicated with an arrow.
Abbreviation: MTHFR, methylenetetrahydrofolate reductase.
Figure 2 The patient has a homozygous MTHFR gene mutation c.677C>T (p.A222V).

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.