Literature DB >> 14981712

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

Joseph G Gleeson1, Lesley C Keeler, Melissa A Parisi, Sarah E Marsh, Phillip F Chance, Ian A Glass, John M Graham, Bernard L Maria, A James Barkovich, William B Dobyns.   

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. Copyright 2003 Wiley-Liss, Inc.

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Year:  2004        PMID: 14981712     DOI: 10.1002/ajmg.a.20437

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  82 in total

1.  Interpeduncular heterotopia in Joubert syndrome: a previously undescribed MR finding.

Authors:  I Harting; U Kotzaeridou; A Poretti; A Seitz; J Pietz; M Bendszus; E Boltshauser
Journal:  AJNR Am J Neuroradiol       Date:  2011-06-02       Impact factor: 3.825

2.  Joubert syndrome type I: neuroimaging findings in addition to the 'molar tooth' sign.

Authors:  Satvinder Kaur; Ketan Kulkarni
Journal:  BMJ Case Rep       Date:  2010-04-29

Review 3.  Joubert Syndrome and related disorders.

Authors:  Francesco Brancati; Bruno Dallapiccola; Enza Maria Valente
Journal:  Orphanet J Rare Dis       Date:  2010-07-08       Impact factor: 4.123

4.  Joubert syndrome associated with severe central sleep apnea.

Authors:  Lisa Wolfe; Hüseyin Lakadamyali; Gökhan M Mutlu
Journal:  J Clin Sleep Med       Date:  2010-08-15       Impact factor: 4.062

5.  AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome.

Authors:  M A Parisi; D Doherty; M L Eckert; D W W Shaw; H Ozyurek; S Aysun; O Giray; A Al Swaid; S Al Shahwan; N Dohayan; E Bakhsh; O S Indridason; W B Dobyns; C L Bennett; P F Chance; I A Glass
Journal:  J Med Genet       Date:  2005-09-09       Impact factor: 6.318

6.  Autofluorescence and High-Resolution OCT Findings Revealed Ciliopathy in Senior-Loken Syndrome.

Authors:  Wener Cella; Luiz H Lima; Nan-Kai Wang; Joaquin Tosi; Lawrence A Yannuzzi; Stephen H Tsang
Journal:  Ophthalmic Surg Lasers Imaging       Date:  2010-03-09

Review 7.  Genetics of the polymicrogyria syndromes.

Authors:  A Jansen; E Andermann
Journal:  J Med Genet       Date:  2005-05       Impact factor: 6.318

8.  Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variability.

Authors:  Izak J Bisschoff; Christine Zeschnigk; Denise Horn; Brigitte Wellek; Angelika Rieß; Maja Wessels; Patrick Willems; Peter Jensen; Andreas Busche; Jens Bekkebraten; Maya Chopra; Hanne Dahlgaard Hove; Christina Evers; Ketil Heimdal; Ann-Sophie Kaiser; Erdmut Kunstmann; Kristina Lagerstedt Robinson; Maja Linné; Patricia Martin; James McGrath; Winnie Pradel; Katrina E Prescott; Bernd Roesler; Gorazd Rudolf; Ulrike Siebers-Renelt; Nataliya Tyshchenko; Dagmar Wieczorek; Gerhard Wolff; William B Dobyns; Deborah J Morris-Rosendahl
Journal:  Hum Mutat       Date:  2012-10-17       Impact factor: 4.878

Review 9.  Joubert syndrome: insights into brain development, cilium biology, and complex disease.

Authors:  Dan Doherty
Journal:  Semin Pediatr Neurol       Date:  2009-09       Impact factor: 1.636

10.  Cilia localization is essential for in vivo functions of the Joubert syndrome protein Arl13b/Scorpion.

Authors:  Neil A Duldulao; Sunjin Lee; Zhaoxia Sun
Journal:  Development       Date:  2009-12       Impact factor: 6.868

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