Literature DB >> 20658556

Multiple cranial nerve neuropathies, microcephaly, neurological degeneration, and "fork and bracket sign" in the MRI: a distinct syndrome.

André Mégarbané1, Nathalie Dorison, Diana Rodriguez, Jean Tamraz.   

Abstract

We report on two sibs with an elongated face with reduced expression, microcephaly, strabismus, wide philtrum, mild joint laxity, thumb sign, bilateral foot drop, and fixed pes cavus, absent tendinous reflexes, an unsteady gait, quick fatigue, slightly diminished limb muscle strength more pronounced distally, abnormalities of cranial nerves III, IV, VII, and most probably VI, and slowness in ideation. Previously unknown findings referred to as the "fork sign" at the pontine level and the "bracket sign" at the mesencephalic level were documented by magnetic resonance imaging. Differential diagnoses and the possibility of a hitherto unreported syndrome are discussed. Copyright 2010 Wiley-Liss, Inc.

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Year:  2010        PMID: 20658556     DOI: 10.1002/ajmg.a.33417

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


  4 in total

1.  SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvement.

Authors:  Andreea Manole; Alejandro Horga; Josep Gamez; Nuria Raguer; Maria Salvado; Beatriz San Millán; Carmen Navarro; Alan Pittmann; Mary M Reilly; Henry Houlden
Journal:  Neurogenetics       Date:  2016-12-22       Impact factor: 2.660

2.  A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs).

Authors:  Davide Pareyson; Tanya Stojkovic; Mary M Reilly; Sarah Leonard-Louis; Matilde Laurà; Julian Blake; Yesim Parman; Esra Battaloglu; Meriem Tazir; Mounia Bellatache; Nathalie Bonello-Palot; Nicolas Lévy; Sabrina Sacconi; Raquel Guimarães-Costa; Sharham Attarian; Philippe Latour; Guilhem Solé; André Megarbane; Rita Horvath; Giulia Ricci; Byung-Ok Choi; Angelo Schenone; Chiara Gemelli; Alessandro Geroldi; Mario Sabatelli; Marco Luigetti; Lucio Santoro; Fiore Manganelli; Aldo Quattrone; Paola Valentino; Tatsufumi Murakami; Steven S Scherer; Lois Dankwa; Michael E Shy; Chelsea J Bacon; David N Herrmann; Alberto Zambon; Irene Tramacere; Chiara Pisciotta; Stefania Magri; Stefano C Previtali; Alessandra Bolino
Journal:  Ann Neurol       Date:  2019-05-27       Impact factor: 11.274

3.  "Fork and bracket" syndrome expands the spectrum of SBF1-related sensory motor polyneuropathies.

Authors:  Marta Romani; Cybel Mehawej; Tommaso Mazza; Andre Mégarbané; Enza Maria Valente
Journal:  Neurol Genet       Date:  2016-03-03

4.  Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunction.

Authors:  Beatrice Berti; Giovanna Longo; Francesco Mari; Stefano Doccini; Ilaria Piccolo; Maria Alice Donati; Francesca Moro; Renzo Guerrini; Filippo M Santorelli; Vittoria Petruzzella
Journal:  BMC Med Genomics       Date:  2021-06-12       Impact factor: 3.063

  4 in total

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