Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Más filtros

Banco de datos
País/Región como asunto
Tipo del documento
Asunto de la revista
País de afiliación
Intervalo de año de publicación
1.
Sensors (Basel) ; 24(14)2024 Jul 10.
Artículo en Inglés | MEDLINE | ID: mdl-39065851

RESUMEN

BACKGROUND: People with blindness and intellectual disability can have problems locating, identifying, and retrieving objects needed for daily activities (e.g., clothes and food items) from familiar storage contexts, such as cupboards and cabinets. OBJECTIVE: This preliminary study assessed a technological system designed to help three people with those problems improve their performance. METHODS: The technological system, which involved the use of tags with radio frequency identification codes, a smartphone, and a tag reader, aimed to guide the participants in searching and retrieving objects from three different storage units. In practice, the system provided different feedbacks depending on whether the participants were searching (a) in a wrong storage unit, (b) in a wrong shelf/drawer of the right storage unit, or (c) in the right shelf/drawer of the right storage unit. RESULTS: All participants were successful in retrieving objects correctly with the technological system. The results also showed that (a) the participants preferred using the system over a control strategy, (b) were able to switch on and off the system independently, and (b) staff rated the system positively. CONCLUSIONS: These preliminary findings suggest that the system might be a useful support tool for people with blindness and intellectual disability.


Asunto(s)
Ceguera , Discapacidad Intelectual , Dispositivos de Autoayuda , Humanos , Ceguera/rehabilitación , Masculino , Adulto , Femenino , Teléfono Inteligente , Dispositivo de Identificación por Radiofrecuencia/métodos , Prueba de Estudio Conceptual
2.
Am J Med Genet A ; 164A(12): 3042-51, 2014 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-25255904

RESUMEN

Since 2005, the Pediatric Clinic of Maternal-Infantile Sciences Institute in Ancona, in collaboration with the Lega del Filo d'Oro in Osimo, has been taking care of 35 patients with clinical and molecular diagnosis of CHARGE syndrome. Our investigation is the largest Italian cohort study of CHARGE patients. CHARGE syndrome is a multiple malformation syndrome involving ocular coloboma, heart defects, choanal atresia, retardation of growth and\or development, genital anomalies and\or urinary and ear abnormalities which leads to visual-auditory disabilities, cognitive impairment and behavioral abnormalities. Our purpose is to expand the knowledge of this syndrome by reviewing this group of affected patients in order to delineate in detail the natural history of the disease, and in particular to define the cognitive and motor profiles using an Italian questionnaire called "Progress Guide". Our main results show that Italian CHARGE patients have more delayed development in their physical abilities or skills with respect to normal patients. In particular, the delay is statistically significant in regard to self-care skills (worse toileting, better washing) and the communication skill (language). On the other hand, the expressive skills are still preserved. When patients are considered according to their age (≤3 years) and (>3 years), the older ones have more delayed development than the younger ones when compared with healthy individuals of the same age.


Asunto(s)
Síndrome CHARGE/diagnóstico , Síndrome CHARGE/epidemiología , Síndrome CHARGE/patología , Trastornos del Conocimiento/patología , Trastornos de la Destreza Motora/patología , Fenotipo , Factores de Edad , Síndrome CHARGE/genética , Estudios de Cohortes , Femenino , Humanos , Italia/epidemiología , Masculino , Mutación/genética , Encuestas y Cuestionarios
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA