Brown–Vialetto–Van Laere syndrome: Egyptian case reportFootnote

Available online 3 December 2011

Footnote

Peer review under responsibility of Alexandria University Faculty of Medicine.

References

• S.A.HawkinsN.C.NevinA.E.HardingPontobulbar palsy and neurosensory deafness (Brown–Vialetto–Van Laere syndrome) with possible autosomal dominant inheritanceJ Med Genet271990176
   PubMed Web of Science ®Google Scholar
• H.V.PrabhuM.J.S.BrownBrown–Vialetto–Van Laere syndrome: a rare syndrome in otologyJ Laryngol Otol11962005470472
   Web of Science ®Google Scholar
• C.H.BrownInfantile amyotrophic lateral sclerosis of the family typeJ Nerv Ment Dis211894707716 Quoted from Ref. [6]
   Google Scholar
• E.VialettoContributo alla forma ereditaria della paralisi bulbare progressiveRiv Sper Freniat401936124 Quoted from Ref. [6]
   Google Scholar
• J.Van LaereParalysie bulbo-pontine chronique progressive familiale avec surdité. Un cas de syndrome de KlippelRev Neurol1151966289295 Quoted in Ref. [6]
   PubMedGoogle Scholar
• S.SathasivamBrown–Vialetto–Van Laere syndrome reviewOrphanet J Rare Dis320089
   PubMed Web of Science ®Google Scholar
• K.A.VoudrisA.SkardoutsouA.VagiakouInfantile progressive bulbar palsy with deafnessBrain Dev242002732735
   PubMed Web of Science ®Google Scholar
• A.MégarbanéI.DesguerresE.RizkallahV.DelagueR.NabboutA.BaroisBrown–Vialetto–Van Laere syndrome in a large inbred Lebanese family: confirmation of autosomal recessive inheritance?Am J Med Genet922000117121
   PubMed Web of Science ®Google Scholar
• D.De GrandisP.PassadoreM.ChinagliaF.BrazzoR.RavenniP.CudiaClinical features and neurophysiological follow-up in a case of Brown–Vialetto–Van Laere syndromeNeuromusc Disord152005565568
   Web of Science ®Google Scholar
• José AugustoMalheirosSarah TeixeiraCamargosJosé Teotoniode OliveiraFrancisco E.C.CardosoAbrazilian family with Brown Vialetto Van Laere syndrome with autosomal recessive inheritanceArq Neuropsiquiatr65120073235
   Web of Science ®Google Scholar
• M.A.McShaneS.BoydB.HardingE.M.BrettJ.WilsonProgressive bulbar paralysis of childhood. A reappraisal of Fazio-Londe diseaseBrain115199218891900
   PubMed Web of Science ®Google Scholar
• C.W.CremersB.G.Ter HaarT.J.Van RensThe Nathalie syndrome. A new hereditary syndromeClin Genet81975330340
   PubMed Web of Science ®Google Scholar
• E.BoltshauserW.LangT.SpillmanE.HofHereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophyJ Med Genet261989105108
   PubMed Web of Science ®Google Scholar
• E.MeenakshisundaramK.JagannathanB.RamamurthyClinical pattern of motor neuron disease seen in younger age groups in MadrasNeurol India18Suppl 31970109112
   Google Scholar
• A.NaliniB.K.YaminiN.GayatriK.ThennarasuR.GopeFamilial Madras motor neuron disease (FMMND): study of 15 families from southern IndiaJ Neurol Sci2502006140146
   PubMed Web of Science ®Google Scholar
• Konstantinos A.VoudrisAngelikiSkardoutsouEleni A.VagiakouInfantile progressive bulbar palsy with deafness case reportBrain Dev242002732735
   PubMed Web of Science ®Google Scholar
• P.GreenM.WisemanY.J.CrowH.HouldenS.RiphagenJ.P.LinBrown–Vialetto–Van Laere Syndrome, a ponto-bulbar palsy with deafness, is caused by mutations in C20orf54Am J Hum Genet862010485489
   PubMed Web of Science ®Google Scholar
• A.M.BoschN.G.AbelingL.IJlstH.KnoesterW.L.PolA.E.StroomerBrown–Vialetto–Van Laere and Fazio Londe syndrome is associated with a riboflavin transporter defect mimicking mild MADD: a new inborn error of metabolism with potential treatmentJ Inherit Metab Dis342011159164
   PubMed Web of Science ®Google Scholar
• V.GallaiJ.M.HockadayJ.T.HughesD.J.LaneD.R.OppenheimerG.RushworthPonto-bulbar palsy with deafness (Brown–Vialetto–Van Laere syndrome). A report on three casesJ Neurol Sci501981259275
   PubMed Web of Science ®Google Scholar
• G.PiccoloE.MarchioniM.MaurelliF.SimonettiF.BizzettiF.SavoldiRecovery from respiratory muscle failure in a sporadic case of Brown–Vialetto–Van Laere syndrome with unusually late onsetJ Neurol2391992355356
   Web of Science ®Google Scholar
• S.DiptiA.-M.ChildsJ.H.LivingstonA.K.AggarwalM.MillerC.WilliamsBrown–Vialetto–Van Laere syndrome: variability in age at onset and disease progression highlighting the phenotypic overlap with Fazio-Londe diseaseBrain Dev272005443446
   Web of Science ®Google Scholar
• Ö.F.AydinD.ÖzcelikelN.SenbilY.K.Y.GürerBrown–Vialetto–Van Laere syndrome; the first Turkish caseActa Neurol Belg1042004111113
   PubMed Web of Science ®Google Scholar
• S.SathasivamS.O'sullivanA.NicolsonP.J.TilleyP.J.ShawBrown- Vialetto-Van Laere syndrome: case report and literature reviewAmyotroph Lateral Scler Other Motor Neuron Disord142000277281
   Web of Science ®Google Scholar
• R.J.DavenportC.J.MumfordThe Brown–Vialetto–Van Laere syndrome: a case report and literature reviewEur J Neurol119945154
   Google Scholar
• R.RamachandranNairM.ParameswaranA.S.GirijaVialetto–Van Laere syndrome in two sisters born to consanguineous parentsPediatr Neurol302004354355
   Web of Science ®Google Scholar
• R.KoulR.JainA.ChackoA.AlfutaisiJ.HashimJ.ChackoPontobulbar palsy and neurosensory deafness (Brown–Vialetto–Van Laere syndrome) with hyperintense brainstem nuclei on magnetic resonance imaging: new finding in three siblingsJ Child Neurol212006523525
   PubMed Web of Science ®Google Scholar
• J.M.AbarbanelP.AshbyA.Marquez-JulioK.R.ChapmanBulbo-pontine paralysis with deafness: the Vialetto–Van Laere syndromeCan J Neurol Sci181991349351
   Web of Science ®Google Scholar
• H.NemotoS.KonnoN.NomotoN.WakataT.KuriharaA case of Brown–Vialetto–Van Laere (BVVL) syndrome in JapanClin Neurol452005357361
   Google Scholar
• J.MiaoH.LiH.LinC.SuY.LiuG.LeiSevere sleep disordered breathing in a patient with Brown–Vialetto–Van Laere syndrome: polysomnographic findingsJ Neurol Sci2632007214217
   Web of Science ®Google Scholar
• D.A.FrancisJ.R.PonsfordC.M.WilesP.K.ThomasL.W.DuchenCase report. Brown–Vialetto–Van Laere syndromeNeuropathol Appl Neurobiol1919939194
   PubMed Web of Science ®Google Scholar
• A.F.KocH.BozdemirY.SaricaMental retardation associated with Brown–Vialetto–Van Laere syndromeAmyotroph Lateral Scler Other Motor Neuron Disord4120035253
   Web of Science ®Google Scholar
• J.A.MalheirosS.T.CamargosJ.T.de OliveiraF.E.C.CardosoA Brazilian family with Brown–Vialetto–Van Laere syndrome with autosomal recessive inheritanceArq Neuropsiquiatr6520073235
   Web of Science ®Google Scholar
• V.GallaiJ.M.HockadayJ.T.HughesD.J.LaneD.R.OppenheimerG.RushworthPonto-bulbar palsy with deafness (Brown–Vialetto–Van Laere syndrome)J Neurol Sci501981259275
   PubMed Web of Science ®Google Scholar