RESUMEN
The aim of this study was to determine the association of benign recurrent vertigo (BRV) and migraine, using standardized questionnaire-based interview of 208 patients with BRV recruited through a University Neurotology clinic. Of 208 patients with BRV, 180 (87%) met the International Classification of Headache Disorders 2004 criteria for migraine: 112 migraine with aura (62%) and 68 without aura (38%). Twenty-eight (13%) did not meet criteria for migraine. Among patients with migraine, 70% experienced headache, one or more auras, photophobia, or auditory symptoms with some or all of their vertigo attacks, meeting the criteria for definite migrainous vertigo. Thirty per cent never experienced migraine symptoms concurrent with vertigo attacks. These met criteria for probable migrainous vertigo. Among patients without migraine, 21% experienced either photophobia or auditory symptoms with some or all of their vertigo attacks; 79% experienced only isolated vertigo. The age of onset and duration of vertigo attacks did not differ significantly between patients with (34 +/- 1.2 years) and patients without migraine (31 +/- 3.0 years). In patients with migraine, the age of onset of migraine headache preceded the onset of vertigo attacks by an average of 14 years and aura preceded vertigo by 8 years. The most frequent duration of vertigo attacks was between 1 h and 1 day. Benign recurrent vertigo is highly associated with migraine, but a high proportion of patients with BRV and migraine never have migraine symptoms during their vertigo attacks. Other features such as age of onset and duration of vertigo are similar between patients with or without migraine.
Asunto(s)
Trastornos Migrañosos/complicaciones , Vértigo/complicaciones , Adulto , Edad de Inicio , Femenino , Humanos , Masculino , Trastornos Migrañosos/epidemiología , Prevalencia , Encuestas y Cuestionarios , Vértigo/epidemiologíaRESUMEN
OBJECTIVES: To prospectively follow patients with vestibular neuritis (VN), to compare the recovery pattern of canal and otolith dysfunction, and to determine which tests best predict symptom recovery. METHODS: Between March 2006 and December 2006, 51 consecutive patients with unilateral VN were enrolled within 7 days of onset (average 3 days). Otolith function tests included ocular torsion (OT), subjective visual vertical (SVV), and vestibular evoked myogenic potential (VEMP), and canal function tests included head-shaking nystagmus (HSN), caloric stimulation, and head-thrust testing. Patients returned for two follow-up evaluations at approximately 1 week and 6 weeks after the initial evaluation. RESULTS: On the first examination, all patients had abnormal HSN, caloric, and head-thrust test results, and at least one otolith-related test abnormality: abnormal tilt of SVV (48/51, 94%), abnormal OT (42/51, 82%), or abnormal VEMPs (25/51, 49%). The degree of SVV tilts correlated with the degree of OT for one or both eyes (p < 0.05). Skew deviation was observed in 7 patients (14%), and a complete ocular tilt reaction was detected in only 2 patients. On follow-up, otolith test results returned to normal more rapidly than canal test results. The head-thrust test was the best predictor of symptom recovery. Eighty percent of patients who continued to report dizziness at the last follow-up visit had a positive head-thrust test result, whereas only 10% of patients who were not dizzy had a positive head-thrust test result. CONCLUSION: Otolith-related test abnormalities improve more rapidly than canal-related test abnormalities after vestibular neuritis. If patients have a positive head-thrust test result on follow-up, they are more likely to be dizzy.
Asunto(s)
Membrana Otolítica/fisiopatología , Recuperación de la Función , Pruebas de Función Vestibular/métodos , Neuronitis Vestibular/diagnóstico , Neuronitis Vestibular/fisiopatología , Vestíbulo del Laberinto/fisiopatología , Adulto , Anciano , Anciano de 80 o más Años , Pruebas Calóricas/estadística & datos numéricos , Mareo/diagnóstico , Mareo/etiología , Mareo/fisiopatología , Femenino , Movimientos de la Cabeza , Humanos , Masculino , Persona de Mediana Edad , Valor Predictivo de las Pruebas , Pronóstico , Estudios Prospectivos , Sensibilidad y Especificidad , Pruebas de Función Vestibular/normasRESUMEN
CONCLUSION: Coexistent migraine affects relevant clinical features of patients with Ménière's disease (MD). OBJECTIVE: Epidemiological studies have shown an association between migraine and MD. We sought to determine whether the coexistence of migraine affects any clinical features in patients with MD. PATIENTS AND METHODS: In this retrospective case-control study of University Neurotology Clinic patients, 50 patients meeting 1995 AAO-HNS criteria for definite MD were compared to 18 patients meeting the same criteria in addition to the 2004 IHS criteria for migraine (MMD). All had typical low frequency sensorineural hearing loss and episodes of rotational vertigo. Outcome measures included: sex, age of onset of episodic vertigo or fluctuating hearing loss, laterality of hearing loss, aural symptoms, caloric responses, severity of hearing loss, and family history of migraine, episodic vertigo or hearing loss. RESULTS: Age of onset of episodic vertigo or fluctuating hearing loss was significantly lower in patients with MMD (mean +/- 1.96*SE = 37.2 +/- 6.3 years) than in those with MD (mean +/- 1.96*SE = 49.3 +/- 4.4 years). Concurrent bilateral aural symptoms and hearing loss were seen in 56% of MMD and 4% of MD patients. A family history of episodic vertigo was seen in 39% of MMD and 2% of MD patients.
Asunto(s)
Enfermedad de Meniere/fisiopatología , Trastornos Migrañosos/fisiopatología , Adolescente , Adulto , Anciano , Niño , Femenino , Humanos , Masculino , Enfermedad de Meniere/complicaciones , Persona de Mediana Edad , Trastornos Migrañosos/complicaciones , Estudios RetrospectivosRESUMEN
Primary episodic ataxias are autosomal dominant channelopathies that manifest as attacks of imbalance and incoordination. Mutations in two genes, KCNA1 and CACNA1A, cause the best characterized and account for the majority of identified cases of episodic ataxia. We summarize current knowledge of clinical and genetic diagnosis, genotype-phenotype correlations, pathophysiology and treatment of episodic ataxia syndromes. We focus on unresolved issues including phenotypic and genetic heterogeneity, lessons from animal models and technological advancement, rationale and feasibility of various treatment strategies, and shared mechanisms underlying episodic ataxia and other far more prevalent paroxysmal conditions such as epilepsy and migraine.
Asunto(s)
Ataxia Cerebelosa/diagnóstico , Animales , Canales de Calcio/genética , Ataxia Cerebelosa/tratamiento farmacológico , Ataxia Cerebelosa/genética , Diagnóstico Diferencial , Modelos Animales de Enfermedad , Genotipo , Humanos , Canal de Potasio Kv.1.1/genética , Ratones , Mutación , FenotipoRESUMEN
We describe four families with late onset episodic vertical oscillopsia and progressive gait ataxia. Probands presented between the ages of 40 and 64 years with initial symptoms of episodic vertical oscillopsia and interictal downbeat nystagmus. A mild gait ataxia developed over several years. Triggers included physical exertion, alcohol and caffeine. Patients did not respond to acetazolamide. Genetic screening for episodic ataxia types 1 and 2, and spinocerebellar ataxias 1, 2, 3 and 6 were negative. Using ancestral identity by descent analysis and dense single nucleotide polymorphism (SNP) genotyping throughout the genome, an interval of 28.6 cM (approximately 14.2 Mb) on chromosome 13q12.11-q13.3, composed of 1259 SNPs, was shared between affected individuals in two of the four families and highlighted a region of suggestive linkage (LOD >2.7).
Asunto(s)
Cromosomas Humanos Par 13/genética , Ataxia de la Marcha/genética , Ligamiento Genético/genética , Trastornos de la Motilidad Ocular/genética , Ilusiones Ópticas , Ataxias Espinocerebelosas/genética , Adulto , Anciano , Femenino , Efecto Fundador , Ataxia de la Marcha/diagnóstico , Carga Genética , Genotipo , Haplotipos , Humanos , Masculino , Persona de Mediana Edad , Nistagmo Congénito/diagnóstico , Nistagmo Congénito/genética , Trastornos de la Motilidad Ocular/diagnóstico , Polimorfismo de Nucleótido Simple/genética , Ataxias Espinocerebelosas/diagnóstico , SíndromeRESUMEN
BACKGROUND: Familial hemiplegic migraine (FHM) is an unusual migraine syndrome characterised by recurrent transient attacks of unilateral weakness or paralysis as part of the migraine aura. Genetically and clinically heterogeneous, FHM1 is caused by mutations in CACNA1A and FHM2 by mutations in ATP1A2. AIM: Three children with prolonged hemiplegia were tested for mutations in CACNA1A or ATP1A2. METHODS: Mutations in CACNA1A and ATP1A2 were screened for by denaturing high performance liquid chromatography and confirmed by sequencing. Expression studies were performed to characterise the functional consequences of these mutations. RESULTS: No mutation was found in the FHM1 gene while three mutations were identified in the FHM2 gene. All three mutations were missense: two were novel and one was de novo; none was found in controls. Functional studies in HeLa cells showed complete loss of mutant pump function without interfering with the wild-type pump, consistent with haploinsufficiency. CONCLUSION: We identified novel disease causing mutations in the FHM2 gene. Genetic screening for FHM should be considered in a child with prolonged hemiplegia even if there is no prior history or family history of migraine or hemiplegic episodes.
Asunto(s)
Migraña con Aura/genética , Mutación Missense , ATPasa Intercambiadora de Sodio-Potasio/genética , Niño , Análisis Mutacional de ADN , Femenino , Pruebas Genéticas , Humanos , MasculinoRESUMEN
We studied a family with nonprogressive congenital ataxia (NPCA) previously reported in 1985. Follow-up evaluation documented a nonprogressive course. Older family members developed ataxic spells and vertical oscillopsia triggered by stress and exercise. Linkage analysis using a 10K single-nucleotide polymorphism array found suggestive linkage to four loci on chromosomes 1q44, 5q35.1-35.3, 7q36.2-36.3, and 9q31.2-32 and ruled out linkage to the NPCA locus on 3p, proving genetic heterogeneity for autosomal dominant NPCA.
Asunto(s)
Ataxia Cerebelosa/genética , Cerebelo/anomalías , Predisposición Genética a la Enfermedad/genética , Polimorfismo Genético/genética , Adulto , Ataxia Cerebelosa/diagnóstico , Ataxia Cerebelosa/fisiopatología , Cerebelo/patología , Cerebelo/fisiopatología , Niño , Preescolar , Trastornos de los Cromosomas/genética , Mapeo Cromosómico , Cromosomas Humanos Par 1/genética , Cromosomas Humanos Par 5/genética , Cromosomas Humanos Par 7/genética , Cromosomas Humanos Par 9/genética , Análisis Mutacional de ADN , Femenino , Estudios de Seguimiento , Genes Dominantes/genética , Pruebas Genéticas , Humanos , Patrón de Herencia/genética , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Mutación/genética , LinajeRESUMEN
OBJECTIVE: To determine the frequency of cerebellar infarction mimicking vestibular neuritis (VN), the pattern of clinical presentation, and the territory of the cerebellar infarction when it simulates VN. METHODS: We studied 240 consecutive cases of isolated cerebellar infarction in the territories of the cerebellar arteries diagnosed by brain MRI from the acute stroke registry at the Keimyung University Dongsan Medical Center. RESULTS: We identified 25 patients (10.4%) with isolated cerebellar infarction who had clinical features suggesting VN. Two types of cerebellar infarction simulating VN were found: isolated spontaneous prolonged vertigo with imbalance as a sole manifestation of cerebellar infarction (n = 24) and isolated spontaneous prolonged vertigo with imbalance as an initial manifestation of cerebellar infarction (n = 1) followed by delayed neurologic deficits 2 days after the onset. The cerebellar infarction territory most commonly involved was the medial branch of the posterior inferior cerebellar artery territory (24/25: 96%), followed by the anterior inferior cerebellar artery territory (1/25: 4%). None of patients with infarcts in the territory of the superior cerebellar artery or multiple cerebellar arteries showed isolated spontaneous prolonged vertigo. CONCLUSIONS: Cerebellar infarction simulating vestibular neuritis is more common than previously thought. Early recognition of the pseudo-vestibular neuritis of vascular cause may allow specific management.
Asunto(s)
Cerebelo/irrigación sanguínea , Infarto/epidemiología , Infarto/patología , Vértigo/epidemiología , Vértigo/patología , Neuronitis Vestibular/patología , Adulto , Anciano , Anciano de 80 o más Años , Arterias/patología , Enfermedades Cerebelosas/diagnóstico , Enfermedades Cerebelosas/epidemiología , Cerebelo/patología , Comorbilidad , Diagnóstico Diferencial , Femenino , Humanos , Incidencia , Corea (Geográfico)/epidemiología , Masculino , Persona de Mediana Edad , Reproducibilidad de los Resultados , Estudios Retrospectivos , Medición de Riesgo/métodos , Factores de Riesgo , Sensibilidad y Especificidad , Neuronitis Vestibular/epidemiologíaRESUMEN
Horizontal gaze palsy with progressive scoliosis (HGPPS) is caused by mutations in the ROBO3 gene, critical for the crossing of long ascending medial lemniscal and descending corticospinal tracts in the medulla. Diffusion tensor imaging in a patient with HGGPS revealed the absence of major pontine crossing fiber tracts and no decussation of the superior cerebellar peduncles. Mutations in the ROBO3 gene lead to a widespread lack of crossing fibers throughout the brainstem.
Asunto(s)
Encefalopatías/genética , Tronco Encefálico/patología , Predisposición Genética a la Enfermedad , Receptores Inmunológicos/genética , Adulto , Encefalopatías/patología , Análisis Mutacional de ADN , Imagen de Difusión por Resonancia Magnética , Salud de la Familia , Femenino , Humanos , Masculino , Mutación , Linaje , Receptores de Superficie Celular , Escoliosis/genéticaRESUMEN
Spinocerebellar ataxia type 2 (SCA2) has protean manifestations, and a clinical marker of progression is needed. Although MRI is a promising tool, it is unclear whether the degree of atrophy shown on MRI is correlated with clinical dysfunction. Here the authors used high-resolution volumetric MRI analysis to show that cerebellar and pontine volumes specifically and closely correlate with functional staging scores.
Asunto(s)
Cerebelo/patología , Imagen por Resonancia Magnética , Puente/patología , Ataxias Espinocerebelosas/diagnóstico , Ataxias Espinocerebelosas/fisiopatología , Adulto , Anciano , Atrofia , Estudios de Casos y Controles , Evaluación de la Discapacidad , Femenino , Humanos , Persona de Mediana EdadAsunto(s)
Ataque Isquémico Transitorio/fisiopatología , Nistagmo Patológico/fisiopatología , Arteria Vertebral/fisiopatología , Insuficiencia Vertebrobasilar/fisiopatología , Vértigo/fisiopatología , Arteria Basilar/patología , Arteria Basilar/fisiopatología , Vértebras Cervicales/patología , Vértebras Cervicales/fisiopatología , Descompresión Quirúrgica/normas , Diagnóstico Diferencial , Oído Interno/irrigación sanguínea , Oído Interno/fisiopatología , Movimientos de la Cabeza/fisiología , Humanos , Ataque Isquémico Transitorio/diagnóstico , Ataque Isquémico Transitorio/etiología , Enfermedades del Laberinto/etiología , Enfermedades del Laberinto/fisiopatología , Enfermedades del Laberinto/cirugía , Nistagmo Patológico/diagnóstico , Nistagmo Patológico/etiología , Rotación/efectos adversos , Síndrome , Arteria Vertebral/anomalías , Arteria Vertebral/patología , Insuficiencia Vertebrobasilar/patología , Insuficiencia Vertebrobasilar/cirugía , Vértigo/diagnóstico , Vértigo/etiologíaAsunto(s)
Vasos Sanguíneos/patología , Hemangioma Cavernoso del Sistema Nervioso Central/genética , Proteínas Asociadas a Microtúbulos/genética , Paraparesia/genética , Proteínas Proto-Oncogénicas/genética , Neoplasias de la Médula Espinal/genética , Médula Espinal/patología , Adulto , Empalme Alternativo/genética , Vasos Sanguíneos/fisiopatología , Análisis Mutacional de ADN , Salud de la Familia , Femenino , Predisposición Genética a la Enfermedad/genética , Hemangioma Cavernoso del Sistema Nervioso Central/fisiopatología , Hemangioma Cavernoso del Sistema Nervioso Central/cirugía , Heterocigoto , Humanos , Proteína KRIT1 , Masculino , Mutación/genética , Procedimientos Neuroquirúrgicos , Parálisis/genética , Parálisis/fisiopatología , Parálisis/cirugía , Paraparesia/fisiopatología , Paraparesia/cirugía , Linaje , Médula Espinal/irrigación sanguínea , Médula Espinal/fisiopatología , Neoplasias de la Médula Espinal/fisiopatología , Neoplasias de la Médula Espinal/cirugía , Vértebras Torácicas , Resultado del TratamientoRESUMEN
BACKGROUND: Transporters, ion pumps, and ion channels are membrane proteins that regulate selective permeability and maintain ionic gradients across cell membranes. Mutations in CACNA1A encoding a neuronal calcium channel and ATP1A2 encoding an ion pump cause episodic ataxia, hemiplegic migraine, and seizures. Mutant gene products of both CACNA1A and ATP1A2 may affect neurotransmission of glutamate, the most abundant excitatory amino acid neurotransmitter. METHODS: We examined our patient population with episodic ataxia and hemiplegic migraine but with no mutation in either CACNA1A or ATP1A2. We looked for mutations in SLC1A3, which encodes the glutamate transporter excitatory amino acid transporter (EAAT) 1 that is important in removing glutamate from the synaptic cleft. RESULTS: A patient with episodic ataxia, seizures, migraine, and alternating hemiplegia has a heterozygous mutation in SLC1A3 that is not present in his asymptomatic parents and controls. Expression studies of the mutant EAAT1 showed decreased expression of the protein with a markedly reduced capacity for glutamate uptake. When coexpressed, the mutant EAAT1 decreased the activity of wild-type EAAT1 but not of two other transporters EAAT2 or EAAT3, suggesting that mutant EAAT1 specifically multimerizes with wild-type EAAT1 to exert its dominant negative effect. CONCLUSION: Our data show that a heterozygous mutation in EAAT1 can lead to decreased glutamate uptake, which can contribute to neuronal hyperexcitability to cause seizures, hemiplegia, and episodic ataxia.
Asunto(s)
Ataxia/genética , Transportador 1 de Aminoácidos Excitadores/genética , Predisposición Genética a la Enfermedad/genética , Ácido Glutámico/metabolismo , Hemiplejía/genética , Convulsiones/genética , Animales , Ataxia/metabolismo , Ataxia/fisiopatología , Encéfalo/metabolismo , Encéfalo/patología , Encéfalo/fisiopatología , Química Encefálica/genética , Edema Encefálico/genética , Edema Encefálico/metabolismo , Edema Encefálico/patología , Células COS , Niño , Chlorocebus aethiops , Análisis Mutacional de ADN , Femenino , Pruebas Genéticas , Hemiplejía/metabolismo , Hemiplejía/fisiopatología , Heterocigoto , Humanos , Imagen por Resonancia Magnética , Masculino , Mutación/genética , Linaje , Convulsiones/metabolismo , Convulsiones/fisiopatologíaRESUMEN
BACKGROUND: CACNA1A encodes CaV2.1, the pore-forming subunit of P/Q-type voltage-gated calcium channel complexes. Mutations in CACNA1A cause a wide range of neurologic disturbances variably associated with cerebellar degeneration. Functional studies to date focus on electrophysiologic defects that do not adequately explain the phenotypic findings. OBJECTIVE: To investigate whether some missense mutations might interfere with protein folding and trafficking, eventually leading to protein aggregation and neuronal injury. METHODS: The authors studied the functional consequences of two pore missense mutations, C287Y and G293R, in two families with EA2, one newly discovered and the other previously reported. Both mutations caused episodic and interictal ataxia. The biophysical properties of mutant and wild type calcium channels were examined by whole-cell patch-clamp recordings in transfected COS-7 cells. The plasma membrane targeting was visualized by confocal fluorescence imaging on CaV2.1 tagged with green fluorescent protein. RESULTS: The mutant channels exhibited a marked reduction in current expression and deficiencies in plasma membrane targeting. CONCLUSIONS: In addition to altered channel function, the deficiency in protein misfolding and trafficking associated with the C287Y and G293R mutants may contribute to the slowly progressive cerebellar ataxia.
Asunto(s)
Ataxia/genética , Canales de Calcio/genética , Enfermedades Cerebelosas/genética , Trastornos Heredodegenerativos del Sistema Nervioso/genética , Mutación Missense/genética , Adolescente , Adulto , Animales , Ataxia/metabolismo , Ataxia/fisiopatología , Células COS , Membrana Celular/genética , Membrana Celular/metabolismo , Enfermedades Cerebelosas/metabolismo , Enfermedades Cerebelosas/fisiopatología , Chlorocebus aethiops , Análisis Mutacional de ADN , Femenino , Pruebas Genéticas , Proteínas Fluorescentes Verdes , Trastornos Heredodegenerativos del Sistema Nervioso/metabolismo , Trastornos Heredodegenerativos del Sistema Nervioso/fisiopatología , Humanos , Masculino , Persona de Mediana Edad , Técnicas de Placa-Clamp , Linaje , Pliegue de Proteína , Transporte de Proteínas/genéticaRESUMEN
OBJECTIVE: To review the neurologic, neuroradiologic, and electrophysiologic features of autosomal recessive horizontal gaze palsy and progressive scoliosis (HGPPS), a syndrome caused by mutation of the ROBO3 gene on chromosome 11 and associated with defective decussation of certain brainstem neuronal systems. METHODS: The authors examined 11 individuals with HGPPS from five genotyped families with HGPPS. Eight individuals had brain MRI, and six had electrophysiologic studies. RESULTS: Horizontal gaze palsy was fully penetrant, present at birth, and total or almost total in all affected individuals. Convergence, ocular alignment, congenital nystagmus, and vertical smooth pursuit defects were variable between individuals. All patients developed progressive scoliosis during early childhood. All appropriately studied patients had hypoplasia of the pons and cerebellar peduncles with both anterior and posterior midline clefts of the pons and medulla and electrophysiologic evidence of ipsilateral corticospinal and dorsal column-medial lemniscus tract innervation. Heterozygotes were unaffected. CONCLUSIONS: The major clinical characteristics of horizontal gaze palsy and progressive scoliosis were congenital horizontal gaze palsy and progressive scoliosis with some variability in both ocular motility and degree of scoliosis. The syndrome also includes a distinctive brainstem malformation and defective crossing of some brainstem neuronal pathways.
Asunto(s)
Mutación/genética , Malformaciones del Sistema Nervioso/genética , Trastornos de la Motilidad Ocular/fisiopatología , Receptores Inmunológicos/genética , Escoliosis/fisiopatología , Adolescente , Adulto , Tronco Encefálico/anomalías , Tronco Encefálico/fisiopatología , Niño , Preescolar , Trastornos de los Cromosomas/genética , Análisis Mutacional de ADN , Femenino , Genes Recesivos/genética , Pruebas Genéticas , Humanos , Lactante , Imagen por Resonancia Magnética , Masculino , Malformaciones del Sistema Nervioso/diagnóstico , Malformaciones del Sistema Nervioso/fisiopatología , Vías Nerviosas/anomalías , Vías Nerviosas/fisiopatología , Trastornos de la Motilidad Ocular/diagnóstico , Trastornos de la Motilidad Ocular/genética , Linaje , Receptores de Superficie Celular , Escoliosis/genética , SíndromeRESUMEN
Two hereditary ataxia syndromes show distinct profiles of region-specific atrophy and ocular motor deficits. Selective pontine atrophy is associated with slowed saccades in ataxin-2 mutations, and selective floccular atrophy is associated with impaired pursuit and gaze-holding abnormalities in Ca(V)2.1 mutations. Although the flocculus seems to be spared relative to the pons in ataxin-2 mutations, and pursuit and gaze-holding appear to be relatively normal, these can be difficult to assess at the bedside, as corrective saccades are also slow and hard to discern. Here, we show the presence of significant floccular atrophy compared with controls in both ataxin-2 and Ca(V)2.1 mutations, which raises the possibility that abnormalities of smooth pursuit or gaze-holding are present in both conditions.
Asunto(s)
Canales de Calcio/genética , Mutación , Proteínas del Tejido Nervioso/genética , Ataxias Espinocerebelosas/genética , Adulto , Anciano , Ataxinas , Atrofia , Canales de Calcio/fisiología , Movimientos Oculares , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proteínas del Tejido Nervioso/fisiología , Ataxias Espinocerebelosas/patología , Ataxias Espinocerebelosas/fisiopatologíaRESUMEN
BACKGROUND: Of the more than 40 genetically defined dominantly inherited hearing loss syndromes, only a few are associated with bilateral vestibulopathy. No genetic mutations have been identified in families with bilateral vestibulopathy and normal hearing. OBJECTIVE: To perform a genome-wide scan for linkage in four families with dominantly inherited bilateral vestibulopathy. METHODS: Patients in four families reported brief episodes of vertigo followed by imbalance and oscillopsia. Bilateral vestibulopathy was documented with quantitative rotational testing. Most patients with bilateral vestibulopathy also had migraine. A 10 cM genome-wide screen was conducted using 423 microsatellite markers to identify linkage with vestibulopathy. RESULTS: The authors identified a 24 cM region on chromosome 6q suggestive of linkage to vestibulopathy in these four families (maximum lod score of 2.9 at marker D6S1556). A small fifth family with a different phenotype was not linked to this region on chromosome 6q. CONCLUSIONS: This is the first report of linkage in families with dominantly inherited vestibulopathy and normal hearing. Genetic heterogeneity is likely with inherited vestibulopathy.
Asunto(s)
Cromosomas Humanos Par 6/genética , Enfermedades Vestibulares/genética , Femenino , Genes Dominantes , Heterogeneidad Genética , Haplotipos , Humanos , Escala de Lod , Masculino , Repeticiones de Microsatélite , Linaje , Fenotipo , Vértigo/genéticaRESUMEN
OBJECTIVE: To describe the clinical and pathologic features of a new dominantly inherited audiovestibular syndrome. METHODS: History, examination, and audiometric testing in the proband, brother, and son; quantitative rotational testing in the proband and son; histopathology of the cochlea and vestibular labyrinth in the proband; sequencing candidate genes COCH and MYO7A in the brother and son. RESULTS: Affected family members developed slowly progressive hearing loss beginning in their late 30s and progressive imbalance in their early 70s. Three of four affected had brief (minutes) episodes of vertigo typically occurring a few times per year. Auditory and vestibular function testing documented a slowly progressive loss of auditory and vestibular function. Postmortem examination showed a loss of hair cells in the cochlea and vestibular receptor organs. There were no cellular infiltrates or acidophilic deposits. No mutations were found in the COCH or MYO7A genes. CONCLUSIONS: This dominantly inherited audiovestibular syndrome results in a selective loss of hair cells in the auditory and vestibular end organs. Finding the causative gene could have important implications for understanding the pathophysiology of presbycusis and dysequilibrium of aging.