RESUMO
BACKGROUND: Hearing loss with enlarged vestibular aqueduct (EVA) can be inherited as an autosomal recessive trait caused by bi-allelic mutations of SLC26A4. However, many EVA patients have non-diagnostic SLC26A4 genotypes with only one or no detectable mutant alleles. METHODS AND RESULTS: In this study, the authors were unable to detect occult SLC26A4 mutations in EVA patients with non-diagnostic genotypes by custom comparative genomic hybridisation (CGH) microarray analysis or by sequence analysis of conserved non-coding regions. The authors sought to compare the segregation of EVA among 71 families with two (M2), one (M1) or no (M0) detectable mutant alleles of SLC26A4. The segregation ratios of EVA in the M1 and M2 groups were similar, but the segregation ratio for M1 was significantly higher than in the M0 group. Haplotype analyses of SLC26A4-linked STR markers in M0 and M1 families revealed discordant segregation of EVA with these markers in eight of 24 M0 families. CONCLUSION: The results support the hypothesis of a second, undetected SLC26A4 mutation that accounts for EVA in the M1 patients, in contrast to non-genetic factors, complex inheritance, or aetiologic heterogeneity in the M0 group of patients. These results will be helpful for counselling EVA families with non-diagnostic SLC26A4 genotypes.
Assuntos
Perda Auditiva/genética , Proteínas de Membrana Transportadoras/genética , Aqueduto Vestibular/patologia , Estudos de Coortes , Hibridização Genômica Comparativa , DNA/química , DNA/genética , Família , Feminino , Variação Genética , Haplótipos , Humanos , Masculino , Linhagem , Análise de Sequência de DNA , Transportadores de SulfatoRESUMO
Fabry disease, OMIM 301500, is a progressive multisystem storage disorder due to the deficiency of alpha-galactosidase A (GALA). Neurological and vascular manifestations of this disorder with regard to hearing loss have not been analysed quantitatively in large cohorts. We conducted a retrospective cross sectional analysis of hearing loss in 109 male and female patients with Fabry disease who were referred to and seen at the Clinical Center of the National Institutes of Health, Bethesda, MD, USA on natural history and enzyme replacement study protocols. There were 85 males aged 6-58 years (mean 31 years, SD 13) and 24 females aged 22-72 years (mean 42 years, SD 12). All patients underwent a comprehensive audiological evaluation. In addition, cerebral white matter lesions, peripheral neuropathy, and kidney function were quantitatively assessed. HL(95), defined as a hearing threshold above the 95th percentile for age and gender matched normal controls, was present in 56% [95% CI (42.2-67.2)] of the males. Prevalence of HL(95) was lower in the group of patients with residual GALA enzyme activity compared with those without detectable activity (33% versus 63%) HL(95) was present in the low-, mid- and high-frequency ranges for all ages. Male patients with HL(95) had a higher microvascular cerebral white matter lesion load [1.4, interquartile range (IQR) 0-30.1 +/- versus 0, IQR 0-0], more pronounced cold perception deficit [19.4 +/- 5.5 versus 13.5 +/- 5.5 of just noticeable difference (JND) units] and lower kidney function [creatinine: 1.6 +/- 1.2 versus 0.77 +/- 0.2 mg/dl; blood urea nitrogen (BUN): 20.1 +/- 14.1 versus 10.3 +/- 3.28 mg/dl] than those without HL(95) (P < 0.001). Of the females, 38% had HL(95). There was no significant association with cold perception deficit, creatinine or BUN in the females. Word recognition and acoustic reflexes analyses suggested a predominant cochlear involvement. We conclude that hearing loss involving all frequency regions significantly contributes to morbidity in patients with Fabry disease. Our quantitative analysis suggests a correlation of neuropathic and vascular damage with hearing loss in the males. Residual GALA activity appears to have a protective effect against hearing loss.
Assuntos
Doença de Fabry/fisiopatologia , Perda Auditiva/fisiopatologia , Adolescente , Adulto , Idoso , Criança , Estudos Transversais , Orelha Média/fisiopatologia , Doença de Fabry/complicações , Feminino , Perda Auditiva/complicações , Humanos , Idioma , Masculino , Microcirculação , Pessoa de Meia-Idade , Doenças do Sistema Nervoso Periférico/complicações , Doenças do Sistema Nervoso Periférico/fisiopatologia , Testes Psicológicos , Estudos Retrospectivos , Limiar Sensorial , Índice de Gravidade de Doença , Fatores Sexuais , Telencéfalo/irrigação sanguínea , Zumbido/complicações , Zumbido/fisiopatologia , alfa-Galactosidase/metabolismoRESUMO
In 103 patients who underwent placement of 106 percutaneous wire-guided intraaortic balloon catheters between August 1983 and January 1986, all placements were successful and the average duration of counterpulsation was 3.4 +/- 1.6 days. During counterpulsation, 45 patients developed limb ischemia that required premature balloon removal in 29 patients. The development of limb ischemia was significantly related to the presence of diabetes (risk ratio 2.0), peripheral vascular disease (risk ratio 1.9), female gender (risk ratio 1.8) and the presence of a postinsertion ankle-brachial pressure index less than 0.8 (risk ratio 7.9). There was no association between the development of limb ischemia and age, body surface area, balloon size (10.5F/12F) or adequacy of anticoagulation. Fifteen patients underwent vascular surgery for treatment of balloon-related limb ischemia, which was associated with one operative death. Nine patients had persistent limb ischemia (seven asymptomatic, two symptomatic) at the time of hospital discharge. Improvements in wire-guided balloon technology have increased the probability of successful balloon placement over that of surgical placement and have reduced the incidence of major aortic injury, but there is no evidence that these improvements have reduced the incidence of limb ischemia or its sequelae. This should be borne in mind before proceeding with balloon insertion in patients with one or more risk factors for developing limb ischemia.
Assuntos
Cateterismo/efeitos adversos , Extremidades/irrigação sanguínea , Balão Intra-Aórtico/efeitos adversos , Isquemia/etiologia , Idoso , Cateterismo/métodos , Feminino , Humanos , Balão Intra-Aórtico/instrumentação , Balão Intra-Aórtico/métodos , Isquemia/terapia , Masculino , Pessoa de Meia-Idade , Alta do PacienteRESUMO
A 46-year-old woman became deaf after a closed head injury. When a computed tomographic scan failed to disclose the cause, conversion disorder was suspected. Magnetic resonance imaging, however, showed bilateral contusions of the inferior colliculi, providing objective evidence for an organic cause of hearing loss. Auditory brain stem evoked responses and stapedial reflexes also provided objective evidence of brain stem injury. This case illustrates the phenomenon of dorsal midbrain injury after head trauma. It indicates the sensitivity of magnetic resonance imaging for small focal lesions after head trauma, and it demonstrates some difficulties in the diagnosis of "hysterical" deafness.
Assuntos
Concussão Encefálica/complicações , Surdez/etiologia , Potenciais Evocados Auditivos do Tronco Encefálico/fisiologia , Colículos Inferiores/lesões , Concussão Encefálica/diagnóstico , Concussão Encefálica/fisiopatologia , Surdez/fisiopatologia , Feminino , Gadolínio DTPA , Humanos , Aumento da Imagem , Imageamento por Ressonância Magnética , Pessoa de Meia-Idade , Compostos Organometálicos , Ácido PentéticoRESUMO
The use of thrombolytic agents for the treatment of myocardial infarction is increasing. Many community hospitals are infusing SK intravenously and those with cardiac catheterization laboratories often use intracoronary SK and angioplasty. Tissue plasminogen activator is undergoing extensive clinical trials, and reports of this research should add to our knowledge of this new therapy. Recently, benefits from thrombolytic therapy such as increased ejection fraction, improved regional wall motion, and short-term decreases in mortality have been documented. Both the GISSI trial that recruited 11,712 patients in Italy and the Netherlands trial documented significant short-term decreases in mortality after therapy with SK compared with control groups. As this information reaches the medical community, we may see an increase in the use of thrombolytic therapy during acute myocardial infarction. Additionally, community education service organizations should reemphasize the importance of seeking help early after the signs and symptoms of acute myocardial infarction appear to promote early treatment and potential salvage of greater amounts of myocardium. The long-term prognosis of patients who have been successfully reperfused and the best management after thrombolytic therapy is not yet known. Future problems and benefits from this therapy are still to be determined.
Assuntos
Infarto do Miocárdio/tratamento farmacológico , Estreptoquinase/uso terapêutico , Ativador de Plasminogênio Tecidual/uso terapêutico , Ensaios Clínicos como Assunto , HumanosRESUMO
In addition to an individual's academic or educational preparation for a specific job or vocation, the importance of physical readiness has been recognized in the past decade. Physical readiness is particularly needed for individuals injured on the job. Work conditioning and work hardening programs have been developed by the health care community in response to this need. An understanding of the characteristics basic to work conditioning and hardening includes awareness of programmatic and philosophical differences between work programs, knowledge of the interdisciplinary team approach, the powerful rehabilitative tool of communication used by work programs particularly for goal formation, and awareness of each team member's role.
Assuntos
Serviços de Saúde do Trabalhador/organização & administração , Planejamento de Assistência ao Paciente , Equipe de Assistência ao Paciente/organização & administração , Reabilitação Vocacional/métodos , Humanos , Masculino , Pessoa de Meia-IdadeAssuntos
Perda Auditiva Neurossensorial/diagnóstico , Perda Auditiva Neurossensorial/genética , Proteínas de Membrana Transportadoras/genética , Mutação , Aqueduto Vestibular/anormalidades , Adolescente , Adulto , Criança , Pré-Escolar , Feminino , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Linhagem , Fenótipo , Transportadores de Sulfato , SíndromeAssuntos
Perda Auditiva Neurossensorial , Judeus/genética , Retinose Pigmentar , Doenças Vestibulares , Adulto , Idoso , Europa Oriental/etnologia , Feminino , Genótipo , Perda Auditiva Neurossensorial/diagnóstico , Perda Auditiva Neurossensorial/etnologia , Perda Auditiva Neurossensorial/genética , Homozigoto , Humanos , Masculino , Proteínas de Membrana/genética , Pessoa de Meia-Idade , Mutação , Linhagem , Fenótipo , Retinose Pigmentar/diagnóstico , Retinose Pigmentar/etnologia , Retinose Pigmentar/genética , Síndrome , Doenças Vestibulares/diagnóstico , Doenças Vestibulares/etnologia , Doenças Vestibulares/genéticaRESUMO
The purpose of this study was to compare the sensitivity of the ABR wave V latency-intensity (L-I) function to that of Alternate Binaural Loudness Balance, Loudness Discomfort Level, and Acoustic Reflex Threshold tests in identifying sensory hearing losses. Five audiometric groups were tested by each procedure. The groups included subjects with normal hearing, and with conductive, high-frequency sensory, flat sensory, and retrocochlear hearing losses. The ability of each test to separate sensory from retrocochlear impairments was investigated. A positive discriminator for cochlear impairments was of particular interest. A combination of wave V L-I slope at lower intensities and the dB HL value that separates steep and shallow slopes of the L-I function appears to meet this objective.
Assuntos
Cóclea , Perda Auditiva Neurossensorial/diagnóstico , Testes Auditivos/métodos , Adolescente , Adulto , Feminino , Testes Auditivos/instrumentação , Humanos , Doenças do Labirinto/diagnóstico , Masculino , Pessoa de Meia-IdadeRESUMO
Language dominance and factors that influence language lateralization were investigated in right-handed, neurologically normal subjects (n = 100) and right-handed epilepsy patients (n = 50) using functional MRI. Increases in blood oxygenation-dependent signal during a semantic language activation task relative to a non-linguistic, auditory discrimination task provided an index of language system lateralization. As expected, the majority of both groups showed left hemisphere dominance, although a continuum of activation asymmetry was evident, with nearly all subjects showing some degree of right hemisphere activation. Using a categorical dominance classification, 94% of the normal subjects were considered left hemisphere dominant and 6% had bilateral, roughly symmetric language representation. None of the normal subjects had rightward dominance. There was greater variability of language dominance in the epilepsy group, with 78% showing left hemisphere dominance, 16% showing a symmetric pattern and 6% showing right hemisphere dominance. Atypical language dominance in the epilepsy group was associated with an earlier age of brain injury and with weaker right hand dominance. Language lateralization in the normal group was weakly related to age, but was not significantly related to sex, education, task performance or familial left-handedness.