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1.
Clin Genet ; 91(4): 529-535, 2017 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-27716896

RESUMEN

The best known café-au-lait syndrome is neurofibromatosis type 1 (NF1). Legius syndrome (LS) is another, rarer syndrome with café-au-lait macules (CALMs). In young patients their clinical picture is often indistinguishable. We investigated the presence of choroidal abnormalities in syndromes with CALMs as a candidate tool for a more efficient diagnosis. Thirty-four patients with NF1 (14 with a truncating mutation, 14 with a non-truncating mutation and 6 with unknown mutation) and 11 patients with LS. All patients underwent an ophthalmological examination. Infrared images were performed. Choroidal nodules were diagnosed in 65% of the NF1 group. About 71% of NF1 patients with a truncating mutation and 50% of patients with a non-truncating mutation were found to have nodules. Choroidal nodules were seen in 18% of the LS patients, never more than one nodule/eye was detected in this group. Choroidal nodules are more abundantly present in NF1 genotypes with truncating mutations. In contrast, the number of choroidal nodules in LS is comparable with their presence in healthy individuals. Especially at an early age, when the clinical picture is incomplete, the detection of choroidal nodules is of diagnostic value, and helps in an appropriate genetic counselling and follow-up. These results support the suggestion to include choroidal nodules to the diagnostic criteria for NF1.


Asunto(s)
Manchas Café con Leche/diagnóstico , Coroides/fisiopatología , Diagnóstico Diferencial , Neurofibromatosis 1/diagnóstico , Proteínas Adaptadoras Transductoras de Señales , Manchas Café con Leche/genética , Manchas Café con Leche/fisiopatología , Asesoramiento Genético , Humanos , Péptidos y Proteínas de Señalización Intracelular/genética , Proteínas de la Membrana/genética , Neurofibromatosis 1/genética , Neurofibromatosis 1/fisiopatología , Agudeza Visual/genética
2.
J Intellect Disabil Res ; 57(9): 874-86, 2013 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-23095048

RESUMEN

BACKGROUND: Neurofibromatosis type 1 (NF1) is a common inherited autosomal dominant condition, characterised by multiple café-au-lait macules, axillary and/or inguinal freckling, iris Lisch nodules and tumours of the nervous system such as neurofibromas and optic pathway gliomas. At the same time, NF1 is frequently associated with intellectual disabilities across several neuropsychological domains. Existing neuropsychological data in NF1 adults are limited and sometimes contradictory. Moreover, most studies use a non-IQ-controlled norm group for comparison. This study sought to investigate specific neuropsychological characteristics in intellectual abilities unrelated to the global intellectual capacity. METHOD: Twenty NF1 adults and an IQ-, age- and gender-matched control group completed a comprehensive neuropsychological test battery composed of specific cognitive tests investigating visual-spatial abilities and memory, auditory memory, selective and sustained attention and executive functioning. A short version of the Wechsler Adult Intelligence Scale - III was also administered to both groups. RESULTS: Norm comparison showed that both groups perform poorly on most neuropsychological functions, except for sustained attention. However, comparison with the IQ-matched control group showed significantly lower scores on visual-spatial abilities and memory, on auditory working memory and on tests for cognitive flexibility in NF1 adults. Nevertheless, as the significant difference in average estimated IQ score between the NF1 group and the selected control group almost reaches the 5% significance level, further analysis is needed to include IQ as a covariate. Eventually, problems in visual-spatial skills and auditory long-term memory seem to be specific NF1-related deficits, while problems in attention and executive functioning are particularly related to their general lowered intellectual abilities. CONCLUSION: Taking into account that primary visual perception problems could be part of a more general central coherence deficit while interpreting auditory memory problems as possibly related to deficits in language use and comprehension, this idea also fits with the observation of several problems in social information processing and functioning of NF1 persons.


Asunto(s)
Trastornos del Conocimiento/etiología , Trastornos del Conocimiento/psicología , Neurofibromatosis 1/complicaciones , Neurofibromatosis 1/psicología , Adolescente , Adulto , Atención , Niño , Función Ejecutiva , Femenino , Humanos , Inteligencia , Masculino , Memoria a Largo Plazo , Memoria a Corto Plazo , Pruebas Neuropsicológicas , Desempeño Psicomotor , Escalas de Wechsler
3.
Rev. Clín. Ortod. Dent. Press ; 10(3): 121-125, jun.-jul. 2011. ilus
Artículo en Portugués | LILACS, BBO - Odontología | ID: lil-602607

RESUMEN

Submersão, infraoclusão e impacção são termos utilizados para definir quando um dente se encontra aquém do plano oclusal, o que pode ser observado em diferentes graus. Na dentição decídua, essa anomalia acomete com mais frequência os segundos molares e a anquilose dentoalveolar é a etiologia mais aceita. Os dentes submersos impactados são fatores locais desencadeantes de má oclusão e, portanto, torna-se importante o diagnóstico precoce a fim de se evitarem danos no desenvolvimento normal da oclusão. A conduta clínica é definida de acordo com as características de cada caso e varia de um tratamento mais conservador ao mais radical, como as exodontias dos dentes envolvidos. Este trabalho tem como objetivo relatar o caso clínico de um paciente com submersão severa dos segundos molares decíduos, sendo que um dos molares em total submersão se encontrava com suspeita de lesão cariosa.


Asunto(s)
Humanos , Masculino , Niño , Anquilosis del Diente , Diente Impactado/cirugía , Diente Impactado/etiología
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