This Article Full Text (PDF) References Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Add to Saved Citations Download to citation manager Request Permissions Request Reprints Add to My Marked Citations Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Citing Articles via Scopus Google Scholar Articles by Fluss, J. Articles by Raybaud, C. Search for Related Content PubMed PubMed Citation Articles by Fluss, J. Articles by Raybaud, C. Social Bookmarking                         What's this?

Molar Tooth Sign in Fetal Brain Magnetic Resonance Imaging Leading to the Prenatal Diagnosis of Joubert Syndrome and Related Disorders

Division of Pediatric Neurology The Hospital for Sick Children University of Toronto

Susan Blaser, MD

Division of Neuroradiology Department of Medical Imaging The Hospital for Sick Children University of Toronto

David Chitayat, MD

Division of Clinical and Metabolic Genetics The Hospital for Sick Children University of Toronto, Department of Obstetrics and Gynecology The Prenatal Diagnosis and Medical Genetics Program Mount Sinai Hospital University of Toronto

Hani Akoury, MD

Department of Obstetrics and Gynecology Women's College Campus Sunnybrook and Women's Health Sciences Centre University of Toronto

Phyllis Glanc, MD

Department of Radiology Women's College Campus Sunnybrook and Women's Health Sciences Centre University of Toronto

Martin Skidmore, MD

Department of Newborn and Developmental Pediatrics Women's College Campus Sunnybrook and Women's Health Sciences Centre University of Toronto

Charles Raybaud, MD

Division of Neuroradiology Department of Medical Imaging The Hospital for Sick Children University of Toronto Toronto, Ontario, Canada, charles. raybaud{at}sickkids.ca

Joubert syndrome is a rare autosomal recessive disorder characterized by ataxia, developmental delay, and oculomotor and respiratory abnormalities in relation to cerebellar vermian and midbrain dysgenesis. The midbrain dysgenesis is responsible for the molar tooth sign on axial magnetic resonance imaging (MRI). This classic hallmark of Joubert syndrome has been identified in other disorders sharing overlapping clinical and radiologic features with Joubert syndrome. Recent identification of two different genes points to genetic heterogeneity in this group of disorders, now entitled Joubert syndrome and related disorders, making a genetic prenatal diagnosis not readily available. In addition, fetal ultrasonography lacks sensitivity in regard to posterior fossa malformation. Fetal MRI is now acknowledged as the method of choice to delineate posterior fossa malformation in a fetus. The identification of a molar tooth sign has, however, rarely been documented by a fetal brain MRI. We report a case of Joubert syndrome diagnosed prenatally using fetal MRI. We also discuss the etiology of Joubert syndrome in view of the recent genetic advances and murine models of cerebellar dysgenesis. (J Child Neurol 2006;21:320—324; DOI 10.2310/7010.2006.00075).

Journal of Child Neurology, Vol. 21, No. 4, 320-324 (2006)
DOI: 10.1177/08830738060210041001


CiteULike    Complore    Connotea    Del.icio.us    Digg    Reddit    Technorati    Twitter    What's this?

This article has been cited by other articles:

				A. Poretti, U. Brehmer, I. Scheer, V. Bernet, and E. Boltshauser Prenatal and Neonatal MR Imaging Findings in Oral-Facial-Digital Syndrome Type VI AJNR Am. J. Neuroradiol., June 1, 2008; 29(6): 1090 - 1091. [Abstract] [Full Text] [PDF]

				M. S. Zaki, A. Abdel-Aleem, G. Abdel-Salam, S. E. Marsh, J. L. Silhavy, A. J. Barkovich, M. E. Ross, S. N. Saleem, W. B. Dobyns, and J. G. Gleeson The molar tooth sign: A new Joubert syndrome and related cerebellar disorders classification system tested in Egyptian families Neurology, February 12, 2008; 70(7): 556 - 565. [Abstract] [Full Text] [PDF]