U.S. flag

An official website of the United States government

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.

Adam MP, Feldman J, Mirzaa GM, et al., editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2024.

Cover of GeneReviews®

GeneReviews® [Internet].

Show details
Figure 1.

Figure 1.

Magnetic resonance imaging of individuals with MECR-related neurologic disorder showing hyperintense T2-weighted and FLAIR signals within the basal ganglia

A. T2-weighted axial section demonstrating hyperintense pallidal signal (arrow) (Family G, Patient II:1) [Author, unpublished observation]

B. T2-weighted axial section demonstrating hyperintense signal in both pallidum and putamen (arrows) (Family G, Patient II:6) [Author, unpublished observation]

C. Flair axial section demonstrating hyperintense signal in both putamen and caudate (arrows) (Family C, Patient II:8) [Heimer et al 2016]

From: MECR-Related Neurologic Disorder

Copyright © 1993-2024, University of Washington, Seattle. GeneReviews is a registered trademark of the University of Washington, Seattle. All rights reserved.

GeneReviews® chapters are owned by the University of Washington. Permission is hereby granted to reproduce, distribute, and translate copies of content materials for noncommercial research purposes only, provided that (i) credit for source (http://www.genereviews.org/) and copyright (© 1993-2024 University of Washington) are included with each copy; (ii) a link to the original material is provided whenever the material is published elsewhere on the Web; and (iii) reproducers, distributors, and/or translators comply with the GeneReviews® Copyright Notice and Usage Disclaimer. No further modifications are allowed. For clarity, excerpts of GeneReviews chapters for use in lab reports and clinic notes are a permitted use.

For more information, see the GeneReviews® Copyright Notice and Usage Disclaimer.

For questions regarding permissions or whether a specified use is allowed, contact: ude.wu@tssamda.

GeneReviews by Title

Views

  • Cite this Page
  • PDF version of this page (575K)

Bulk Download

GeneReviews Links

Related information

  • OMIM
    Related OMIM records
  • PMC
    PubMed Central citations
  • PubMed
    Links to PubMed
  • Gene
    Locus Links

Similar articles in PubMed

  • Review SLC6A3-Related Dopamine Transporter Deficiency Syndrome.[GeneReviews(®). 1993]
    Review SLC6A3-Related Dopamine Transporter Deficiency Syndrome.
    Spaull RVV, Kurian MA. GeneReviews(®). 1993
  • Review ATP1A3-Related Neurologic Disorders.[GeneReviews(®). 1993]
    Review ATP1A3-Related Neurologic Disorders.
    Brashear A, Sweadner KJ, Cook JF, Swoboda KJ, Ozelius L. GeneReviews(®). 1993
  • Review WARS2 Deficiency.[GeneReviews(®). 1993]
    Review WARS2 Deficiency.
    Mroczek M, Busra A, Houlden H, Efthymiou S, Nagy S. GeneReviews(®). 1993
  • Review SLC39A14 Deficiency.[GeneReviews(®). 1993]
    Review SLC39A14 Deficiency.
    Tuschl K, Gregory A, Meyer E, Clayton PT, Hayflick SJ, Mills PB, Kurian MA. GeneReviews(®). 1993
  • Review VPS13A Disease.[GeneReviews(®). 1993]
    Review VPS13A Disease.
    Peikert K, Dobson-Stone C, Rampoldi L, Miltenberger-Miltenyi G, Neiman A, De Camilli P, Hermann A, Walker RH, Monaco AP, Danek A. GeneReviews(®). 1993
See reviews...See all...

Recent Activity

ClearTurn OffTurn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...