Literature DB >> 10508989

Cerebello-oculo-renal syndromes including Arima, Senior-Löken and COACH syndromes: more than just variants of Joubert syndrome.

D Satran1, M E Pierpont, W B Dobyns.   

Abstract

Cerebellar vermis hypoplasia (CVH) is part of many different malformation syndromes, especially Joubert syndrome. However, the nosology of these disorders remains uncertain. We reviewed reports of 100 children with cerebellar vermis hypoplasia, and ocular or renal involvement. Although the status of the upper brainstem was not adequately documented in most of these patients, some had hypoplasia and dysplasia of the ponto-mesencephalic isthmus and the superior portion of the cerebellar vermis, which results in a "molar tooth" sign on MRI scan. Several distinct syndromes were apparent among this group. We conclude that (a) hypoplasia of the cerebellar vermis, especially the anterior vermis, is often associated with a complex brainstem malformation; (b) the latter comprises a "molar tooth" brainstem and vermis hypoplasia-dysplasia malformation complex; (c) this complex may include the Dandy-Walker malformation, occipital cephalocele, and some abnormalities of the cerebrum as evidenced by frequent mental retardation; and (d) the "molar tooth" sign or malformation is causally heterogeneous as it occurs in several distinct malformation syndromes including Joubert syndrome, Arima syndrome, Senior-Löken syndrome, COACH syndrome, and probably familial juvenile nephronophthisis. Copyright 1999 Wiley-Liss, Inc.

Entities:  

Mesh:

Year:  1999        PMID: 10508989

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  41 in total

Review 1.  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

Review 2.  Cilia in cell signaling and human disorders.

Authors:  Neil A Duldulao; Jade Li; Zhaoxia Sun
Journal:  Protein Cell       Date:  2010-08-28       Impact factor: 14.870

3.  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

4.  Neurological picture. Mid-brain molar tooth sign: expanding the clinical spectrum.

Authors:  J N Panicker; B Jyothi; K P Sreekumar
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-01       Impact factor: 10.154

5.  Diffusion tensor imaging in Joubert syndrome.

Authors:  A Poretti; E Boltshauser; T Loenneker; E M Valente; F Brancati; K Il'yasov; T A G M Huisman
Journal:  AJNR Am J Neuroradiol       Date:  2007-09-26       Impact factor: 3.825

Review 6.  Clinical and molecular features of Joubert syndrome and related disorders.

Authors:  Melissa A Parisi
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

Review 7.  Liver and kidney disease in ciliopathies.

Authors:  Meral Gunay-Aygun
Journal:  Am J Med Genet C Semin Med Genet       Date:  2009-11-15       Impact factor: 3.908

8.  Analysis and classification of cerebellar malformations.

Authors:  Sandeep Patel; A James Barkovich
Journal:  AJNR Am J Neuroradiol       Date:  2002-08       Impact factor: 3.825

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.  MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement.

Authors:  Francesco Brancati; Miriam Iannicelli; Lorena Travaglini; Annalisa Mazzotta; Enrico Bertini; Eugen Boltshauser; Stefano D'Arrigo; Francesco Emma; Elisa Fazzi; Romina Gallizzi; Mattia Gentile; Damir Loncarevic; Vlatka Mejaski-Bosnjak; Chiara Pantaleoni; Luciana Rigoli; Carmelo D Salpietro; Sabrina Signorini; Gilda Rita Stringini; Alain Verloes; Dominika Zabloka; Bruno Dallapiccola; Joseph G Gleeson; Enza Maria Valente
Journal:  Hum Mutat       Date:  2009-02       Impact factor: 4.878

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