Search results for "Deaf"

Differentiation in language and gesture use during early bilingual development of hearing children of Deaf parents

2014

Hearing children of Deaf parents simultaneously acquire sign language and spoken language, which have many structural differences and represent two different modalities. We video-recorded eight children every six months between the ages of 12 and 24 months during three different play sessions: with their Deaf parent, with the Deaf parent and a hearing adult, and with a hearing adult alone. Additionally, we collected data on their vocabulary development in both sign language and spoken language. Children as young as 12 months old accommodated their language use according to the language(s) of their interlocutor(s). Additionally, the children used a manual modality that included gestures more…

MODELLI DI DEAFFERENTAZIONE SENSORIALE ED ABITUDINE: MODULAZIONE PLASTICA CON RTMS

2012

L'intérêt de l'animation comme support au code de la route pour les candidats sourds

2018

Entretiens Jacques Cartier, LYON, FRANCE, 13-/11/2018 - 14/11/2018; This article focuses on the interest of using dynamic Highway Code learning materials, particularly for deaf people who present low temporal skills. Twenty-one deaf and 24 hearing candidates of Highway Code were involved in a decision-making task. Four types of driving situations (overtaking, insertion on roundabout, insertion on highway and crossing an intersection) from which participants have to decide to go or not to go were presented in two different formats (static vs animated) and in two level of difficulty (simple vs complex). Results showed better performance in animated than in static condition, especially in deaf…

Italian Sign Language and Spoken Italian in contact: an analysis of interactions between Deaf Parents and Hearing Children

1999

This study explores the outcome of the contact between sign language and spoken italian

Una prospettiva storica e pedagogica sulle Lingue dei Segni: riflessioni psicolinguistiche

2021

Da oltre 50 anni, da quando W. Stokoe negli anni '60 individuò in USA i parametri di articolazione delle lingue dei Segni (cfr. Stokoe, 1981), si assiste ad un sempre maggiore interesse nei confronti delle lingue visivo-gestuali delle comunità di sordi, grazie anche agli sviluppi nel campo della psicolinguistica, delle neuroscienze, e delle nuove tecnologie che consentono indagini sul linguaggio e sul funzionamento cerebrale impensabili sino a qualche tempo fa. Può forse sorprendere che, in una prospettiva storica, all'interno del dibattito linguistico-filosofico si può riscontrare un analogo interesse per i sordi e le loro forme di comunicazione soltanto nella seconda metà del sec. XVIII e…

Cause, pathogenesis, clinical manifestations and treatment of meniere's disease and endolymphatic hydrops

2019

Meniere's disease (MD) is characterized by the triad of fluctuating hearing loss, episodic vertigo and tinnitus, and by endolymphatic hydrops found on postmortem examinations. Since the description of endolymphatic hydrops by Hallpike and Cairns all the physiopathology of Meniere's symptoms have been based on assumption that the pathologic lesion was the cause of the symptoms. Paparella came out term and concept towards understanding of a disease was, "pathogenesis," which applies to all otological diseases, in general and in particular within this context of MD, which allows us to better understand this disease. After Schuknecht proposed the theory of membranous rupture causing the mixing …

Meniere's disease: Therapeutic options

2021

Meniere's disease (MD) is characterized by the triad of fluctuating hearing loss, episodic vertigo and tinnitus, and by endolymphatic hydrops found on postmortem examinations. Since the description of endolymphatic hydrops by Hallpike and Cairns, the physiopathology of Meniere's symptoms has been based on assumption that the pathologic lesion was the cause of the symptoms. Schuknecht proposed the theory of membranous rupture causing the mixing up of endolymph and perilymph leading to the occurrence of Meniere's symptoms. Lawrence confirmed this theory with research on experimental animals. In 1995 the AAO-HNS criteria defines "Possible MD (Grade D), Probable MD (Grade C), Definite MD (Grade…

Understanding Deafhood: in search of its meanings.

2013

The authors argue that Deafhood (a term coined by Dr. Paddy Ladd) is an open-ended concept with an essentialist core. They describe how deaf people who have attended their Deafhood lectures and workshops have perceived different aspects of the Deafhood concept, and compare the basic tenets of Deafhood and criticisms on Deafhood to theories and criticisms on feminist essentialisms. The authors find that the vagueness and wideness of the Deafhood concept is one of its strengths, though they also find that it is in some respects problematic to combine and unite ontology and liberation theory in one concept. They further suggest that the ontological aspects of Deafhood need to be foregrounded. …

Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss.

2015

Hearing loss and individual differences in normal hearing both have a substantial genetic basis. Although many new genes contributing to deafness have been identified, very little is known about genes/variants modulating the normal range of hearing ability. To fill this gap, we performed a two-stage meta-analysis on hearing thresholds (tested at 0.25, 0.5, 1, 2, 4, 8 kHz) and on pure-tone averages (low-, medium-and high-frequency thresholds grouped) in several isolated populations from Italy and Central Asia (total N = 2636). Here, we detected two genome-wide significant loci close to PCDH20 and SLC28A3 (top hits: rs78043697, P = 4.71E-10 and rs7032430, P = 2.39E-09, respectively). For both…

Epidemiological study of nonsyndromic hearing loss in Sicilian newborns

2007

Deafness is caused by a variety of facts, genetic and environmental. Regarding the acquired causes, deafness can be the consequence of prenatal infections, acoustic or cerebral trauma, and the use of ototoxic drugs. Deafness can be the only manifestation (nonsyndromic forms) or it may occur together with other phenotypic findings (syndromic forms). The majority of nonsyndromicdeafness has a genetic basis [Van Camp et al., 1997]. In recent years, deafness and hearing loss have assumed a clinical importance in the study of congenital disorders [Morton et al., 1991]. The clinical interest for hearing loss is supported by the social impact that this disorder has; if not treated, delays in the d…