Molar tooth sign of the midbrain-hindbrain junction: occurrence in multiple distinct syndromes.

Abstract

The Molar Tooth Sign (MTS) is defined by an abnormally deep interpeduncular fossa; elongated, thick, and mal-oriented superior cerebellar peduncles; and absent or hypoplastic cerebellar vermis that together give the appearance of a "molar tooth" on axial brain MRI through the junction of the midbrain and hindbrain (isthmus region). It was first described in Joubert syndrome (JS) where it is present in the vast majority of patients with this diagnosis. We previously showed that the MTS is a component of several other syndromes, including Dekaban-Arima (DAS), Senior-Löken, and COACH (cerebellar vermis hypoplasia (CVH), oligophrenia, ataxia, coloboma, and hepatic fibrosis). Here we present evidence that the MTS is seen together with polymicrogyria, Váradi-Papp syndrome (Orofaciodigital VI (OFD VI)), and a new syndrome with encephalocele and cortical renal cysts. We also present a new patient with COACH syndrome plus the MTS. We propose that the MTS is found in multiple distinct clinical syndromes that may share common developmental mechanisms. Proper classification of patients with these variants of the MTS will be essential for localization and identification of mutant genes.

• Authors: Joseph G Gleeson, Lesley C Keeler, Melissa A Parisi, Sarah E Marsh, Phillip F Chance, Ian A Glass, John M Graham Jr, Bernard L Maria, A James Barkovich, William B Dobyns
• Journal: American journal of medical genetics. Part A (Am J Med Genet A) Vol. 125A Issue 2 Pg. 125-34; discussion 117 (03 01 2004) ISSN: 1552-4825 [Print] United States
• PMID: 14981712 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright 2003 Wiley-Liss, Inc.

Topics

• Abnormalities, Multiple (diagnosis)
• Brain (abnormalities, pathology)
• Child
• Child, Preschool
• Developmental Disabilities (diagnosis)
• Female
• Humans
• Infant
• Magnetic Resonance Imaging
• Male
• Pedigree
• Syndrome