Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation Syndrome

M.J. Higley; T.W. Walkiewicz; J.H. Miller; J.G. Curran; R.B. Towbin

doi:10.3174/ajnr.A1969

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Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation Syndrome

M.J. Higley, T.W. Walkiewicz, J.H. Miller, J.G. Curran and R.B. Towbin

American Journal of Neuroradiology February 2011, 32 (2) E23-E25; DOI: https://doi.org/10.3174/ajnr.A1969

M.J. Higley

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T.W. Walkiewicz

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J.H. Miller

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J.G. Curran

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R.B. Towbin

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vol. 32 no. 2 E23-E25

DOI

https://doi.org/10.3174/ajnr.A1969

PubMed

20075099

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American Journal of Neuroradiology

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0195-6108

Online ISSN

1936-959X

History

Received July 20, 2009
Accepted after revision October 26, 2009
Published online February 11, 2011.

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M.J. Higleya,b,
T.W. Walkiewicza,
J.H. Millera,
J.G. Currana and
R.B. Towbina

^aFrom the Department of Radiology (M.J.H., T.W.W., J.H.M., J.G.C., R.B.T.), Phoenix Children's Hospital, Phoenix, Arizona
^bUniversity of Arizona College of Medicine Phoenix (M.J.H.), Phoenix, Arizona.

Please address correspondence to Thomas W. Walkiewicz, MD, Department of Radiology, Phoenix Children's Hospital, 1919 E Thomas Rd, Phoenix, AZ 85016; e-mail: twalkiewicz{at}phoenixchildrens.com

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M.J. Higley, T.W. Walkiewicz, J.H. Miller, J.G. Curran, R.B. Towbin

Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation Syndrome

American Journal of Neuroradiology Feb 2011, 32 (2) E23-E25; DOI: 10.3174/ajnr.A1969

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Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation Syndrome

M.J. Higley, T.W. Walkiewicz, J.H. Miller, J.G. Curran, R.B. Towbin

American Journal of Neuroradiology Feb 2011, 32 (2) E23-E25; DOI: 10.3174/ajnr.A1969

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Genetics of Inner Ear Malformations: A Review

Davide Brotto, Flavia Sorrentino, Roberta Cenedese, Irene Avato, Roberto Bovo, Patrizia Trevisi, Renzo Manara

Audiology Research 2021 11 4
Imaging Findings in Congenital Cranial Dysinnervation Disorders

Rafael Martins Ferreira, Lazaro L.F. Amaral, Marcus V.M. Gonçalves, Katia Lin

Topics in Magnetic Resonance Imaging 2011 22 6
Congenital absence of the bilateral internal carotid artery: a review of the associated (ab)normalities from a newborn status to the eighth decade of life

Ljiljana Vasović, Milena Trandafilović, Slobodan Vlajković, Goran Radenković

Child's Nervous System 2018 34 1
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Ahmed Abdel Khalek Abdel Razek, Hala Maher, Manal Ali Kasem, Eman Helmy

Clinical Imaging 2021 71
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Oncotarget 2017 8 38
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William T. O'Brien, Felice D'Arco, Valeria Onofrj, Bernadette L. Koch

American Journal of Roentgenology 2021 216 4
Syndromic Hearing Loss in Children

Martin Lewis, Caroline D. Robson, Felice D‘Arco

Neuroimaging Clinics of North America 2023 33 4
Bosley–Salih–Alorainy syndrome in patients from India

Siddaramappa J. Patil, Gadabanahalli Ashok Karthik, Gandham SriLakshmi Bhavani, Venkatraman Bhat, Jyoti Matalia, Jhanvi Shah, Anju Shukla, Katta Mohan Girisha

American Journal of Medical Genetics Part A 2020 182 11
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Bilateral Complete Labyrinthine Aplasia with Bilateral Internal Carotid Artery Aplasia, Developmental Delay, and Gaze Abnormalities: A Presumptive Case of a Rare HOXA1 Mutation Syndrome

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