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1.
Arq. neuropsiquiatr ; 74(3): 223-227, Mar. 2016. tab, graf
Article in English | LILACS | ID: lil-777122

ABSTRACT

ABSTRACT Objective The evaluation of selective activation of C-fibers to record evoked potentials using the association of low-power diode laser (810 nm), tiny-area stimulation and skin-blackening. Method Laser-evoked potentials (LEPs) were obtained from 20 healthy young subjects. An aluminum plate with one thin hole was attached to the laser probe to provide tiny-area stimulation of the hand dorsum and the stimulated area was covered with black ink. Results The mean intensity used for eliciting the ultra-late laser-evoked potential (ULEP) was 70 ± 32 mW. All subjects showed a clear biphasic potential that comprised a negative peak (806 ± 61 ms) and a positive deflection (1033 ± 60 ms), corresponding to the ULEP related to C-fiber activation. Conclusion C-fiber-evoked responses can be obtained using a very low-power diode laser when stimulation is applied to tiny areas of darkened skin. This strategy offers a non-invasive and easy methodology that minimizes damage to the tissue.


RESUMO Objetivo Avaliação da ativação de fibras C para o registro de potenciais evocados utilizando-se laser de baixa potência, áreas pequenas de estimulação e escurecimento da pele. Método Potenciais evocados foram obtidos de 20 sujeitos. Uma placa de alumínio com uma pequena abertura foi acoplada à ponteira do laser para estimular área escurecida do dorso da mão. Resultados A intensidade média utilizada para estimulação foi de 70 ± 32 mW. Todos os sujeitos apresentaram respostas claras compreendendo dois picos um negativo (806 ± 61 ms) seguido por outro positivo (1033 ± 60 ms), correspondendo ao potencial evocado tardio por estimulação de fibras C. Conclusão Respostas de fibras C podem ser obtidas utilizando-se laser de baixa potência quando a estimulação é aplicada a pequenas áreas de pele escurecida. Esta estratégia oferece uma metodologia não invasiva que minimiza danos teciduais.


Subject(s)
Humans , Male , Female , Adult , Nociceptors/drug effects , Evoked Potentials, Somatosensory/radiation effects , Lasers, Semiconductor , Nerve Fibers/radiation effects , Reaction Time
2.
Arq. neuropsiquiatr ; 66(1): 117-119, mar. 2008. ilus
Article in English | LILACS | ID: lil-479670

ABSTRACT

This is a brief review of the literature focused on the articles that formed the basis for the classification of the nerve fibers. Mention is also made to the origin of the nomenclature of the different motoneurons (a, b and g).


Os autores fazem uma breve revisão da literatura com foco nos artigos que deram origem à classificação das fibras nervosas. É também mencionada no texto a origem da nomenclatura dos diferentes neurônios motores (a, b and g).


Subject(s)
History, 20th Century , Humans , Nerve Fibers/classification , Neuroanatomy/history
3.
Int. braz. j. urol ; 33(6): 815-821, Nov.-Dec. 2007. ilus, tab
Article in English | LILACS | ID: lil-476646

ABSTRACT

OBJECTIVE: Somatosensory evoked potential (SSEP) is an electrophysiological test used to evaluate sensory innervations in peripheral and central neuropathies. Pudendal SSEP has been studied in dysfunctions related to the lower urinary tract and pelvic floor. Although some authors have already described technical details pertaining to the method, the standardization and the influence of physiological variables in normative values have not yet been established, especially for women. The aim of the study was to describe normal values of the pudendal SSEP and to compare technical details with those described by other authors. MATERIALS AND METHODS: The clitoral sensory threshold and pudendal SSEP latency was accomplished in 38 normal volunteers. The results obtained from stimulation performed on each side of the clitoris were compared to ages, body mass index (BMI) and number of pregnancies. RESULTS: The values of clitoral sensory threshold and P1 latency with clitoral left stimulation were respectively, 3.64 ± 1.01 mA and 37.68 ± 2.60 ms. Results obtained with clitoral right stimulation were 3.84 ± 1.53 mA and 37.42 ± 3.12 ms, respectively. There were no correlations between clitoral sensory threshold and P1 latency with age, BMI or height of the volunteers. A significant difference was found in P1 latency between nulliparous women and volunteers who had been previously submitted to cesarean section. CONCLUSIONS: The SSEP latency represents an accessible and reproducible method to investigate the afferent pathways from the genitourinary tract. These results could be used as normative values in studies involving genitourinary neuropathies in order to better clarify voiding and sexual dysfunctions in females.


Subject(s)
Adult , Aged , Female , Humans , Middle Aged , Pregnancy , Clitoris/physiology , Evoked Potentials, Somatosensory/physiology , Female Urogenital Diseases/diagnosis , Pelvic Floor/physiology , Sensory Thresholds/physiology , Body Mass Index , Clitoris/innervation , Electric Stimulation , Electrodes , Electromyography , Female Urogenital Diseases/physiopathology , Pregnancy Rate , Prospective Studies , Sexual Dysfunction, Physiological/diagnosis
4.
Int. braz. j. urol ; 32(6): 705-712, Nov.-Dec. 2006. ilus, tab, graf
Article in English | LILACS | ID: lil-441371

ABSTRACT

INTRODUCTION & OBJECTIVES: Studies of motor conduction for the efferent functional assessment of the pudendal nerve in women with pelvic dysfunctions have been conducted through researching distal motor latency times. The transrectal approach has been the classic approach for this electrophysiological examination. The objective of the present study is to verify the viability of the transvaginal approach in performing the exam, to establish normal values for this method and to analyze the influence of age, stature and parity in the latency value of normal women. MATERIALS AND METHODS: A total of 23 volunteers without genitourinary pathologies participated in this study. In each, pudendal motor latency was investigated through the transvaginal approach, which was chosen due to patientÆs higher tolerance levels. RESULTS: The motor response represented by registering the M-wave was obtained in all volunteers on the right side (100 percent) and in 13 volunteers on the left side (56.5 percent). The mean motor latency obtained in the right and left was respectively: 1.99 ± 0.41 and 1.92 ± 0.48 milliseconds (ms). There was no difference between the sides (p = 0.66). Latency did not correlate with age, stature or obstetric history. The results obtained in the present study were in agreement with those found by other researchers using the transrectal approach. CONCLUSION: The vaginal approach represents an alternative for pudendal nerve distal motor latency time, with similar results to those achieved through the transrectal approach. Normative values obtained herein might serve as a comparative basis for subsequent physiopathological studies.


Subject(s)
Humans , Female , Adult , Neural Conduction/physiology , Pelvic Floor/innervation , Urinary Incontinence/diagnosis , Anal Canal/innervation , Anal Canal/physiopathology , Electromyography , Reaction Time , Urinary Incontinence/physiopathology , Vagina
5.
Arq. neuropsiquiatr ; 64(3a): 582-584, set. 2006. ilus
Article in English, Portuguese | LILACS | ID: lil-435590

ABSTRACT

Andersen syndrome (AS) is a rare disease characterized by the presence of periodic paralysis (PP), cardiac arrhythmia and dysmorphic abnormalities. We report herein the first Brazilian patient presenting AS who also had obesity, obstructive sleep apnea (OSA) and daytime sleepiness. Clinical and genetic evaluation of six family members demonstrated that four had dysmorphic abnormalities but none had PP or cardiac arrhythmia. Sequencing of KCNJ2 revealed the R218W mutation in the index patient and her 6-year-old daughter, who presented dysmorphic abnormalities (micrognathia, clinodactyly of fourth and fifth fingers, short stature) and OSA. Three relatives had clinodactyly as the only manifestation but the R218W mutation was absent, suggesting that this characteristic may be influenced by another gene. OSA accompanied by dysmorphic features may be related to AS.


A síndrome de Andersen (SA) é doença rara caracterizada pela presença de paralisia periódica (PP), arritmia cardíaca e anormalidades dismórficas. Relatamos o primeiro paciente brasileiro apresentando SA, e que também apresenta obesidade e apnéia obstrutiva do sono (AOS). Avaliações clínica e genética de seis familiares demonstraram que quatro apresentavam alterações dismórficas mas nenhum tinha PP ou arritmia cardíaca. O sequenciamento do gene KCNJ2 revelou a mutação R218W no paciente índex e sua filha de 6 anos, que apresentava alterações dismórficas (micrognatia, clinodactilia do quarto e quinto dedos, baixa estatura) e AOS. Três familiares tinham clinodactilia como única manifestação mas a mutação R218W estava ausente, sugerindo que esta característica seja influenciada por outro gene. A AOS associada a alterações dismórficas pode estar relacionada à SA.


Subject(s)
Humans , Male , Female , Child , Adult , Andersen Syndrome/complications , Andersen Syndrome/genetics , Mutation/genetics , Potassium Channels, Inwardly Rectifying/genetics , Sleep Apnea, Obstructive/complications , Andersen Syndrome/diagnosis , Electrocardiography , Pedigree , Polysomnography
6.
Arq. neuropsiquiatr ; 62(2A): 253-256, jun. 2004. tab
Article in English | LILACS | ID: lil-361350

ABSTRACT

A neuropatia periférica é complicação neurológica comum, podendo ocorrer nas fases assintomáticas e sintomáticas da infecção pelo vírus da imunodeficiência humana (HIV). As síndromes mais comuns são a polineuropatia distal simétrica, polineuropatia desmielinizante inflamatória, polirradiculopatia, mononeuropatia, mononeuropatia múltipla e neuropatia autonômica. OBJETIVO: Avaliar a freqüência da neuropatia periférica em um grupo de pacientes HIV positivo em São Paulo, Brasil. MÉTODO: Em um período de 17 meses, foram avaliados clinicamente 49 pacientes HIV positivos. Foram solicitados exames laboratoriais e eletroneuromiografia (ENMG) para todos os pacientes. RESULTADOS: Foi estabelecido o diagnóstico clínico de neuropatia periférica em 34 (69,4%) dos 49 pacientes. O sinal neurológico mais comum foi a alteração da sensibilidade (97,1%). Treze (33,3%) dos 39 pacientes que realizaram a ENMG tiveram o diagnóstico de neuropatia periférica, sendo a neuropatia sensitivo-motora axonal o achado mais comum. Não foram encontradas alterações significativas nos exames laboratoriais (42 pacientes realizaram os exames), com exceção de quatro pacientes em que o VDRL foi positivo. CONCLUSÃO: A neuropatia periférica foi um achado freqüente no grupo de pacientes HIV positivo estudados clinicamente.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , HIV Seropositivity/epidemiology , Peripheral Nervous System Diseases/epidemiology , Brazil/epidemiology , Electromyography/methods , HIV Seropositivity/complications , HIV Seropositivity/immunology , Prevalence , Peripheral Nervous System Diseases/diagnosis , Peripheral Nervous System Diseases/etiology
7.
Arq. neuropsiquiatr ; 60(3B): 699-701, Sept. 2002. ilus, tab
Article in English | LILACS | ID: lil-325478

ABSTRACT

PURPOSE:This study compared some morphological features of individual rolandic epileptiform discharges, used to obtain an averaged estimate, with those of the resulting estimate. METHOD: Twenty-four averaged discharges from EEGs of 24 children showing rolandic spikes were compared with 480 individual discharges used in the averaging. The analysis was based on the occurrence of tangential dipole and "double spike" patterns. RESULTS: In 15 averaged discharges the tangential dipole pattern was found. Individual spikes used in the averaging process displayed the same pattern in 35-100 percent of them; in the remaining 9 averaged discharges, up to 20 percent of the individual spikes showed the same pattern, although this was not found in the averaged waveforms. "Double spike" pattern was found in 11 of the averaged waveforms and was recognized in 50-100 percent of its individual discharges, whereas up to 45 percent of individual spikes showed this pattern without expression in the averaged waveform. CONCLUSION: When visually analyzing an EEG with rolandic spikes, caution should be exercised in characterizing these patterns, since a few discharges showing them may not be expressed in the averaged waveform and the clinical correlations proposed for these patterns may not apply


Subject(s)
Humans , Child , Action Potentials , Electroencephalography , Epilepsy, Rolandic , Pattern Recognition, Visual
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