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Research ArticlePediatrics

Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients

R. Bhargava, K.J. Au Yong and N. Leonard
American Journal of Neuroradiology February 2014, 35 (2) 402-406; DOI: https://doi.org/10.3174/ajnr.A3680
R. Bhargava
aFrom the Departments of Radiology and Diagnostic Imaging (R.B.)
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K.J. Au Yong
cDepartment of Radiology and Diagnostic Imaging (K.J.A.), McMaster University Medical Centre, McMaster Children's Hospital, Hamilton, Ontario, Canada.
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N. Leonard
bMedical Genetics (N.L.), University of Alberta Hospital, Edmonton, Alberta, Canada
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Article Information

vol. 35 no. 2 402-406
DOI 
https://doi.org/10.3174/ajnr.A3680
PubMed 
23907246

Published By 
American Journal of Neuroradiology
Print ISSN 
0195-6108
Online ISSN 
1936-959X
History 
  • Received April 14, 2013
  • Accepted after revision May 27, 2013
  • Published online February 12, 2014.

Article Versions

  • Latest version (August 1, 2013 - 07:03).
  • You are viewing the most recent version of this article.
Copyright & Usage 
© 2014 by American Journal of Neuroradiology

Author Information

  1. R. Bhargavaa,
  2. K.J. Au Yongc and
  3. N. Leonardb
  1. aFrom the Departments of Radiology and Diagnostic Imaging (R.B.)
  2. bMedical Genetics (N.L.), University of Alberta Hospital, Edmonton, Alberta, Canada
  3. cDepartment of Radiology and Diagnostic Imaging (K.J.A.), McMaster University Medical Centre, McMaster Children's Hospital, Hamilton, Ontario, Canada.
  1. Please address correspondence to Kong Jung Au Yong, MB ChB, MRCS, FRCR, MBA, Department of Radiology and Diagnostic Imaging, McMaster University Medical Centre, McMaster Children's Hospital, 1280 Main St West, Hamilton, ON L8S 4L8, Canada; e-mail: kong.auyong{at}gmail.com
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Cite this article
R. Bhargava, K.J. Au Yong, N. Leonard
Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
American Journal of Neuroradiology Feb 2014, 35 (2) 402-406; DOI: 10.3174/ajnr.A3680

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Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
R. Bhargava, K.J. Au Yong, N. Leonard
American Journal of Neuroradiology Feb 2014, 35 (2) 402-406; DOI: 10.3174/ajnr.A3680
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This article has been cited by the following articles in journals that are participating in Crossref Cited-by Linking.

  • PTEN Hamartoma tumor syndrome in childhood: A review of the clinical literature
    William L. Macken, Marc Tischkowitz, Katherine L. Lachlan
    American Journal of Medical Genetics Part C: Seminars in Medical Genetics 2019 181 4
  • Clinical spectrum of PTEN mutation in pediatric patients. A bicenter experience
    Claudia Ciaccio, Veronica Saletti, Stefano D'Arrigo, Silvia Esposito, Enrico Alfei, Isabella Moroni, Davide Tonduti, Luisa Chiapparini, Chiara Pantaleoni, Donatella Milani
    European Journal of Medical Genetics 2019 62 12
  • A clinical review on megalencephaly
    Piero Pavone, Andrea Domenico Praticò, Renata Rizzo, Giovanni Corsello, Martino Ruggieri, Enrico Parano, Raffaele Falsaperla
    Medicine 2017 96 26
  • Behavioural and psychological features of PTEN mutations: a systematic review of the literature and meta-analysis of the prevalence of autism spectrum disorder characteristics
    Katherine Cummings, Alice Watkins, Chris Jones, Renuka Dias, Alice Welham
    Journal of Neurodevelopmental Disorders 2022 14 1
  • Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome
    Tugce B. Balci, Jorge Davila, Denice Lewis, Addo Boafo, Erick Sell, Julie Richer, Sarah M. Nikkel, Christine M. Armour, Eva Tomiak, Matthew A. Lines, Sarah L. Sawyer
    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 2018 177 1
  • Vascular Anomaly Syndromes in the ISSVA Classification System: Imaging Findings and Role of Interventional Radiology in Management
    Mindy X. Wang, Serageldin Kamel, Khaled M. Elsayes, R. Paul Guillerman, Ahmed Habiba, Lauren Heng, Margarita Revzin, Vincent Mellnick, Ionela Iacobas, Alex Chau
    RadioGraphics 2022 42 6
  • Clinical presentation of PTEN mutations in childhood in the absence of family history of Cowden syndrome
    T. Busa, M. Milh, N. Degardin, N. Girard, S. Sigaudy, M. Longy, S. Olshchwang, H. Sobol, B. Chabrol, N. Philip
    European Journal of Paediatric Neurology 2015 19 2
  • Polymicrogyria is Associated With Pathogenic Variants in PTEN
    Diane D. Shao, Christelle M. Achkar, Abbe Lai, Siddharth Srivastava, Ryan N. Doan, Lance H. Rodan, Allen Y. Chen, Annapurna Poduri, Edward Yang, Christopher A. Walsh
    Annals of Neurology 2020 88 6
  • The Rare Neurocutaneous Disorders
    Felipe S. Barros, Victor Hugo R. Marussi, Lázaro L.F. Amaral, Antônio José da Rocha, Christiane M.S. Campos, Leonardo F. Freitas, Thierry A.G.M. Huisman, Bruno P. Soares
    Topics in Magnetic Resonance Imaging 2018 27 6
  • Distinctive facies, macrocephaly, and developmental delay are signs of a PTEN mutation in childhood
    Kohji Kato, Seiji Mizuno, Mie Inaba, Shinobu Fukumura, Naoko Kurahashi, Koichi Maruyama, Daisuke Ieda, Kei Ohashi, Ikumi Hori, Yutaka Negishi, Ayako Hattori, Shinji Saitoh
    Brain and Development 2018 40 8

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