Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations

M. Elmaleh-Bergès; C. Baumann; N. Noël-Pétroff; A. Sekkal; V. Couloigner; K. Devriendt; M. Wilson; S. Marlin; G. Sebag; V. Pingault

doi:10.3174/ajnr.A3367

Research ArticlePediatrics

Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations

M. Elmaleh-Bergès, C. Baumann, N. Noël-Pétroff, A. Sekkal, V. Couloigner, K. Devriendt, M. Wilson, S. Marlin, G. Sebag and V. Pingault

American Journal of Neuroradiology June 2013, 34 (6) 1257-1263; DOI: https://doi.org/10.3174/ajnr.A3367

M. Elmaleh-Bergès

aFrom the Departments of Pediatric Imaging (M.E.-B., A.S., G.S.)

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

C. Baumann

bClinical Genetics (C.B.)

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

N. Noël-Pétroff

cOtorhinolaryngology (N.N.-P.), Hôpital Robert Debré, Paris, France

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

A. Sekkal

aFrom the Departments of Pediatric Imaging (M.E.-B., A.S., G.S.)

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

V. Couloigner

eDepartment of Otorhinolaryngology (V.C.), Hôpital Necker-Enfants Malades, Paris, France

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

K. Devriendt

dCenter for Human Genetics (K.D.), University Hospitals Leuven, Leuven, Belgium

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

M. Wilson

fDepartment of Clinical Genetics (M.W.), The Children's Hospital at Westmead, Sydney, Australia

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

S. Marlin

gCentre de Référence des Surdités Génétiques (S.M.), Hôpital Armand-Trousseau, Paris, France

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

G. Sebag

aFrom the Departments of Pediatric Imaging (M.E.-B., A.S., G.S.)

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

V. Pingault

hLaboratoire de Biochimie et Génétique (V.P.), AP-HP, Hôpital Henri Mondor–Albert Chenevier, Créteil, France.

Find this author on Google Scholar
Find this author on PubMed
Search for this author on this site

Article
Figures & Data
Supplemental
Info & Metrics
Responses
References
PDF

Submit a Response to This Article

Compose eLetter

Title *

Contents

More information about text formats

Plain text

No HTML tags allowed.
Web page addresses and e-mail addresses turn into links automatically.
Lines and paragraphs break automatically.

Author Information

Contributors
First Name and Middle Initial * First or given name, e.g. 'Peter'. Last Name * Your last, or family, name, e.g. 'MacMoody'. Email Address * Your email address, e.g. higgs-boson@gmail.com Occupation * Your role and/or occupation, e.g. 'Orthopedic Surgeon'. Affiliation * Your organization or institution (if applicable), e.g. 'Royal Free Hospital'.

Statement of Competing Interests

Competing interests? *

Yes

Please describe the competing interests

Vertical Tabs

Jump to comment:

No eLetters have been published for this article.

PreviousNext

In this issue

American Journal of Neuroradiology

Vol. 34, Issue 6

1 Jun 2013

Table of Contents
Index by author

Download PDF

Email Article

Thank you for your interest in spreading the word on American Journal of Neuroradiology.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Your Email *

Your Name *

Send To *

Enter multiple addresses on separate lines or separate them with commas.

You are going to email the following Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations

Message Subject (Your Name) has sent you a message from American Journal of Neuroradiology

Message Body (Your Name) thought you would like to see the American Journal of Neuroradiology web site.

Your Personal Message

CAPTCHA

This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.

Cite this article

M. Elmaleh-Bergès, C. Baumann, N. Noël-Pétroff, A. Sekkal, V. Couloigner, K. Devriendt, M. Wilson, S. Marlin, G. Sebag, V. Pingault

Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations

American Journal of Neuroradiology Jun 2013, 34 (6) 1257-1263; DOI: 10.3174/ajnr.A3367

Citation Manager Formats

BibTeX
Bookends
EasyBib
EndNote (tagged)
EndNote 8 (xml)
Medlars
Mendeley
Papers
RefWorks Tagged
Ref Manager
RIS
Zotero

0 Responses

Respond to this article

Bookmark this article

User Name *

Password *

Remember my user name & password.

Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations

M. Elmaleh-Bergès, C. Baumann, N. Noël-Pétroff, A. Sekkal, V. Couloigner, K. Devriendt, M. Wilson, S. Marlin, G. Sebag, V. Pingault

American Journal of Neuroradiology Jun 2013, 34 (6) 1257-1263; DOI: 10.3174/ajnr.A3367

Share This Article:

Tweet Widget
Facebook Like
Google Plus One

Purchase

Jump to section

Article
Figures & Data
Supplemental
Info & Metrics
Responses
References
PDF

PubMed
Google Scholar

Cited By...

SOX10: 20 years of phenotypic plurality and current understanding of its developmental function
GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing
Olfactory bulb agenesis with normal sexual hormones
Spectrum of Clinical and Associated MR Imaging Findings in Children with Olfactory Anomalies

Crossref (94)
Google Scholar

This article has been cited by the following articles in journals that are participating in Crossref Cited-by Linking.

GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing

Luigi Maione, Andrew A Dwyer, Bruno Francou, Anne Guiochon-Mantel, Nadine Binart, Jérôme Bouligand, Jacques Young

European Journal of Endocrinology 2018 178 3
Hypomyelinating leukodystrophies — unravelling myelin biology

Nicole I. Wolf, Charles ffrench-Constant, Marjo S. van der Knaap

Nature Reviews Neurology 2021 17 2
Hearing loss in Waardenburg syndrome: a systematic review

J. Song, Y. Feng, F.R. Acke, P. Coucke, K. Vleminckx, I.J. Dhooge

Clinical Genetics 2016 89 4
Neurosensory development and cell fate determination in the human cochlea

Heiko Locher, Johan HM Frijns, Liesbeth van Iperen, John CMJ de Groot, Margriet A Huisman, Susana M Chuva de Sousa Lopes

Neural Development 2013 8 1
Lacrimal gland development: From signaling interactions to regenerative medicine

Ankur Garg, Xin Zhang

Developmental Dynamics 2017 246 12
SOX10: 20 years of phenotypic plurality and current understanding of its developmental function

Veronique Pingault, Lisa Zerad, William Bertani-Torres, Nadege Bondurand

Journal of Medical Genetics 2022 59 2
Efficient Generation of Gene-Modified Pigs Harboring Precise Orthologous Human Mutation via CRISPR/Cas9-Induced Homology-Directed Repair in Zygotes

Xiaoyang Zhou, Lulu Wang, Yinan Du, Fei Xie, Liang Li, Yu Liu, Chuanhong Liu, Shiqiang Wang, Shibing Zhang, Xingxu Huang, Yong Wang, Hong Wei

Human Mutation 2016 37 1
The Zebrafish - Disease Models and Chemical Screens

B. Blanco-Sánchez, A. Clément, J.B. Phillips, M. Westerfield

2017 138
Biology of human melanocyte development, Piebaldism, and Waardenburg syndrome

Mohammed D. Saleem

Pediatric Dermatology 2019 36 1
CT findings of the temporal bone in CHARGE syndrome: aspects of importance in cochlear implant surgery

A. C. Vesseur, B. M. Verbist, H. E. Westerlaan, F. J. J. Kloostra, R. J. C. Admiraal, C. M. A. van Ravenswaaij-Arts, R. H. Free, E. A. M. Mylanus

European Archives of Oto-Rhino-Laryngology 2016 273 12

Main menu

User menu

Search

American Journal of Neuroradiology

Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations

Plain text

Vertical Tabs

Jump to comment:

In this issue

Citation Manager Formats

Related Articles

Cited By...

More in this TOC Section

Similar Articles

Indexed Content

Cases

Special Collections

Resources

Multimedia

About Us

American Society of Neuroradiology