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Henricson, Cecilia
Publications (10 of 17) Show all publications
Henricson, C., Frölander, H. E., Möller, C. & Lyxell, B. (2016). Theory-of-mind and cognitive function in adults with Usher and Alström syndromes. Journal of Visual Impairment & Blindness, 110(5), 349-366
Open this publication in new window or tab >>Theory-of-mind and cognitive function in adults with Usher and Alström syndromes
2016 (English)In: Journal of Visual Impairment & Blindness, ISSN 0145-482X, E-ISSN 1559-1476, Vol. 110, no 5, p. 349-366Article in journal (Refereed) Published
Abstract [en]

Objective: Theory-of-Mind (ToM) refers to the ability to impute mental states to one self and to others. ToM was investigated in adults with Usher syndrome type II (USH2) and Alström syndrome (AS) - two syndromes causing acquired deafblindness. The syndromes differ with regard to onset and degree of sensory loss. Individuals with AS in contrast to individuals with USH2 display a high incidence of additional physical diseases. Cognitive shortcomings are generally not observed in USH2 or in AS, but cognitive delay and a delay in receptive language have been reported in AS. The results were compared to adults with normal hearing and vision (NHV).

Methods: Thirteen persons with USH2, 12 persons with AS, and 33 persons with NHV participated. All participants performed a test of working memory capacity and verbal ability. ToM was tested with Happe´s Strange Stories test, taxing the ability to understand the emotions and actions of story characters, comprising a mental condition. The test also include a section of matched stories, tapping verbal problem solving ability in a physical condition, and a set of tasks tapping the ability to recall verbal material.

Results: There were no differences between the three groups in the ability to recall verbal material. Significant differences were however established on working memory, and on verbal problem solving in a physical condition, with higher results for the NHV group. The two groups with deafblindness also displayed poorer ToM performance than the NHV group, by producing fewer correct mental references. The two groups with deafblindness differed from each other also in the ability to produce mental inferences as such, where the USH group outperformed the AS group. Intra-group variability in this ability was also observed within the two syndromal groups. Differences were related to verbal ability, complex working memory capacity, visual status, and to a minor extent auditory capacity. The prevalence and severity of additional physical diseases in AS was not related to ToM performance.

Conclusions: A limited access to information as a function of sensory loss could influence degree of experience of the physical world, but also of social situations and of communication, affecting ToM development negatively. Early loss of visual field and visual acuity was related to ToM performance in individuals with USH2 and AS. Access to information also requires processing skills promoted by effective cognitive skills. Working memory capacity was related to ToM in USH. This relation also points to the contribution of hearing in development of ToM. Differences between the two groups could be a function of genetic conditions, where the gene causing USH2 only affects the ear and the eye, while AS in addition has a multi-systemic pathology with varying onset and degree. Differences in ToM performance in the AS group could however not be directly attributed to health conditions.

Place, publisher, year, edition, pages
AMER FOUNDATION BLIND, 2016
Keywords
Usher syndrome (USH); Alström syndrome (AS); Theory-of-Mind; Deafblindness; physical disorders
National Category
Social Sciences Interdisciplinary Psychology
Identifiers
urn:nbn:se:liu:diva-120113 (URN)000384900000006 ()
Note

Funding agencies: Linnaeus Centre HEAD

Available from: 2015-07-09 Created: 2015-07-09 Last updated: 2018-01-11Bibliographically approved
Henricson, C., Lidestam, B., Lyxell, B. & Moller, C. (2015). Cognitive skills and reading in adults with Usher syndrome type 2. Frontiers in Psychology, 6(326)
Open this publication in new window or tab >>Cognitive skills and reading in adults with Usher syndrome type 2
2015 (English)In: Frontiers in Psychology, ISSN 1664-1078, E-ISSN 1664-1078, Vol. 6, no 326Article in journal (Refereed) Published
Abstract [en]

Objective: To investigate working memory (WM), phonological skills, lexical skills, and reading comprehension in adults with Usher syndrome type 2 (USH2). Design: The participants performed tests of phonological processing, lexical access, WM, and reading comprehension. The design of the test situation and tests was specifically considered for use with persons with low vision in combination with hearing impairment. The performance of the group with USH2 on the different cognitive measures was compared to that of a matched control group with normal hearing and vision (NVH). Study Sample: Thirteen participants with USH2 aged 21-60 years and a control group of 10 individuals with NVH, matched on age and level of education. Results: The group with USH2 displayed significantly lower performance on tests of phonological processing, and on measures requiring both fast visual judgment and phonological processing. There was a larger variation in performance among the individuals with USH2 than in the matched control group. Conclusion: The performance of the group with USH2 indicated similar problems with phonological processing skills and phonological WM as in individuals with long-term hearing loss. The group with USH2 also had significantly longer reaction times, indicating that processing of visual stimuli is difficult due to the visual impairment. These findings point toward the difficulties in accessing information that persons with USH2 experience, and could be part of the explanation of why individuals with USH2 report high levels of fatigue and feelings of stress (Wahlqvist et al., 2013).

Place, publisher, year, edition, pages
Frontiers, 2015
Keywords
deafblindness; Usher syndrome; phonological skill; lexical skill; working memory; reading
National Category
Psychology (excluding Applied Psychology)
Identifiers
urn:nbn:se:liu:diva-117380 (URN)10.3389/fpsyg.2015.00326 (DOI)000351714000001 ()25859232 (PubMedID)
Note

Funding Agencies|Swedish Research Council Forte; Audiological Research Centre in Orebro

Available from: 2015-04-24 Created: 2015-04-24 Last updated: 2017-12-04
Henricson, C., Lyxell, B., Lidestam, B. & Möller, C. (2015). Reading skill in five children with Usher Syndrome type 1 and Cochlear implants.
Open this publication in new window or tab >>Reading skill in five children with Usher Syndrome type 1 and Cochlear implants
2015 (English)Manuscript (preprint) (Other academic)
Abstract [en]

Objective: The aim of this study was to explore and describe reading skill in children with Usher syndrome type 1 and who have cochlear implants (USH1+CI), and to position their performance in relation to that of three control groups: children with normal hearing (NH), children with hearing impairment and hearing aids (HI+HA), and children with other types of deafness and CI (other CI).

Method: Reading comprehension and decoding was measured in five children with USH1+CI in the ages 7.5–16 years. The children participated during a test session of 2–2.5 hours and performed tests including reading skill, WM, phonological skills, and lexical skills.

Results: Four of the children with USH1+CI achieved results similar to those of the control group with NH on the measures of reading skill. One child with USH1+CI performed below all control groups. Three of the children with USH1+CI had high performance on both the measures of phonological skill and on the tests of reading skill. The groups perform similar results on the tests of reading skill.

Conclusions: Three of the children with USH1+CI decode non-words with a phonological decoding strategy, similar to the strategy applied by the control group with NH. Two of the children with USH1+CI relied on an orthographic decoding strategy, possibly relying on other cognitive skills than the phonological strategy.

Keywords
Reading skill; Usher syndrome type 1; Cochlear Implant; phonological skills; working memory
National Category
Social Sciences Interdisciplinary Psychology
Identifiers
urn:nbn:se:liu:diva-120112 (URN)
Available from: 2015-07-09 Created: 2015-07-09 Last updated: 2018-01-11Bibliographically approved
Lyxell, B., Wass, M., Sahlén, B., Uhlén, I., Möller, C., Henricson, C., . . . Mäki-Torkko, E. (2013). Cognitive and communicative development in deaf and hearing-impaired children with cochlear implants and/or hearing-aids. In: : . Paper presented at Second International Conference on Cognitive Hearing Science for Communication, Linköping University, Sweden, June 16-19, 2013. (pp. 114).
Open this publication in new window or tab >>Cognitive and communicative development in deaf and hearing-impaired children with cochlear implants and/or hearing-aids
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2013 (English)Conference paper, Oral presentation with published abstract (Other academic)
Abstract [en]

The purpose of the study was to examine neurophysiological, cognitive and linguistic development in deaf and hearing-impaired children (5–7 years of age) with CI and/or hearingaids and how a phonological intervention programme may influence this development. The deaf and hearing-impaired children were compared with age-matched hearing children. The results reveal that deaf and hearing-impaired children had equivalent or close to equivalent performance levels compared to hearing children for cognitive and linguistic tasks with relatively low demands on phonological processing, whereas there was a substantial and significant difference between the groups for cognitive tasks involving explicit phonological processing. The results indicate that there is a relationship between age at implant and neurophysiological, cognitive and linguistic development, where early implantation promotes faster development. The childrens´ cognitive performance increased as a function of phonological intervention.

National Category
Social Sciences
Identifiers
urn:nbn:se:liu:diva-103053 (URN)
Conference
Second International Conference on Cognitive Hearing Science for Communication, Linköping University, Sweden, June 16-19, 2013.
Available from: 2014-01-12 Created: 2014-01-12 Last updated: 2014-01-28
Möller, C., Lyxell, B., Henricson, C. & Frölander, H.-E. (2013). Different deafblind syndromes and cognitive function: Geno-phenotype correlations and/or sensory deprivation. In: : . Paper presented at Second International Conference on Cognitive Hearing Science for Communication, 16-19 June 2013, Linköping, Sweden (pp. 102-102).
Open this publication in new window or tab >>Different deafblind syndromes and cognitive function: Geno-phenotype correlations and/or sensory deprivation
2013 (English)Conference paper, Oral presentation with published abstract (Other academic)
Abstract [en]

Profound congenital or early aquired deafness is one of the most common severe disabilities (1-2/1000 newborns). Approximately 30% of these children have additional functional disabilities (syndromes). Today nearly 400 syndromes are known, and the most common combination of organ dysfunctions are ear and eye- deafblindness. Many deafblind syndromes have additional dysfunctions of the central nervous system (learning disabilities, delayed mental development etc). Since communication to a large extent is based on an intimate interaction between sight and hearing, this dual sensory loss can if not compensated give rise to severe sensory deprivation and communications problems. We will report results from cognitive studies in Usher and Alström syndrome and some clinical observations regarding CHARGE syndrome. The etiologies of deafblindness with additional cognitive dysfunctions have to be diagnosed very early in order to enhance basic communication skills and habilitation in children with deafblindness have to be enhance the use of multiple sensory capacities such as hearing, vision, tactile, smell, and taste. The importance of early and correct diagnoses for early intervention will be discussed.

National Category
Social Sciences
Identifiers
urn:nbn:se:liu:diva-105151 (URN)
Conference
Second International Conference on Cognitive Hearing Science for Communication, 16-19 June 2013, Linköping, Sweden
Available from: 2014-03-09 Created: 2014-03-09 Last updated: 2014-03-21
Lyxell, B., Wass, M., Sahlén, B., Ibertsson, T., Asker-Árnason, L., Uhlén, I., . . . Möller, C. (2013). Hearing and cognitive development in deaf and hearing-impaired children: effects of intervention. In: Gastone Celesia (Ed.), Disorders of Peripheral and Central Auditory Processing: (pp. 71-80). Amsterdam: Elsevier
Open this publication in new window or tab >>Hearing and cognitive development in deaf and hearing-impaired children: effects of intervention
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2013 (English)In: Disorders of Peripheral and Central Auditory Processing / [ed] Gastone Celesia, Amsterdam: Elsevier, 2013, p. 71-80Chapter in book (Refereed)
Place, publisher, year, edition, pages
Amsterdam: Elsevier, 2013
Series
Handbook of Clinical Neurophysiology, ISSN 1567-4231 ; 10
Keywords
Word deafness, Word deafness in children, Auditory pathways, Ear, Auditory Pathways physiology, Auditory Pathways physiopathology, Hearing Disorders diagnosis
National Category
Social Sciences
Identifiers
urn:nbn:se:liu:diva-100639 (URN)10.1016/B978-0-7020-5310-8.00004-1 (DOI)978-0-7020-5310-8 (ISBN)
Available from: 2013-11-10 Created: 2013-11-10 Last updated: 2014-10-30Bibliographically approved
Henricson, C., Lyxell, B., Möller, C., Lidestam, B. & Wass, M. (2012). Cognitive skills in children with Usher syndrome type 1 and cochlear implants. International Journal of Pediatric Otorhinolaryngology, 76(10), 1449-1457
Open this publication in new window or tab >>Cognitive skills in children with Usher syndrome type 1 and cochlear implants
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2012 (English)In: International Journal of Pediatric Otorhinolaryngology, ISSN 0165-5876, E-ISSN 1872-8464, Vol. 76, no 10, p. 1449-1457Article in journal (Refereed) Published
Abstract [en]

Introduction: Usher syndrome is a genetic condition causing deaf-blindness and is one of the most common causes of syndromic deafness. Individuals with USH1 in Sweden born during the last 15 years have typically received cochlear implants (CI) as treatment for their congenital, profound hearing loss. Recent research in genetics indicate that the cause of deafness in individuals with Usher type 1 (USH1) could be beneficial for the outcome with cochlear implants (CI). This population has not previously been the focus of cognitive research.

Objective: The present study aims to examine the phonological and lexical skills and working memory capacity (WMC) in children with USH1 and CI and to compare their performance with children with NH, children with hearing-impairment using hearing-aids and to children with non-USH1 deafness using CI. The participants were 7 children aged 7-16 years with USH1 and CI.

Methods: The participants performed 10 sets of tasks measuring phonological and lexical skills and working memory capacity.

Conclusions: The results indicate that children with USH1 and CI as a group in general have a similar level of performance on the cognitive tasks as children with hearing impairment and hearing aids. The group with USH1 and CI has a different performance profile on the tests of working memory, phonological skill and lexical skill than children with non-USH1 deafness using CI, on tasks of phonological working memory and phonological skill.

National Category
Social Sciences Interdisciplinary Psychology
Identifiers
urn:nbn:se:liu:diva-78068 (URN)10.1016/j.ijporl.2012.06.020 (DOI)000310048800012 ()
Available from: 2012-06-05 Created: 2012-06-05 Last updated: 2018-01-12
Henricson, C., Lyxell, B. & Lidestam, B. (2012). Fonologiska och lexikala färdigheter samt arbetsminneskapacitet hos barn med ushers syndrom typ 1 och cochleaimplantat. In: : . Paper presented at BARNAS, Örebro, 3-5 september 2012 (pp. 47).
Open this publication in new window or tab >>Fonologiska och lexikala färdigheter samt arbetsminneskapacitet hos barn med ushers syndrom typ 1 och cochleaimplantat
2012 (Swedish)Conference paper, Oral presentation with published abstract (Other academic)
National Category
Social Sciences
Identifiers
urn:nbn:se:liu:diva-102356 (URN)
Conference
BARNAS, Örebro, 3-5 september 2012
Available from: 2013-12-07 Created: 2013-12-07 Last updated: 2014-01-15
Henricson, C., Lyxell, B., Möller, C. & Lidestam, B. (2012). Phonological skills and working memory in children with C1 and Usher typ 1. In: : . Paper presented at Tema Hörsel, March 28-30, Linköping, Sweden.
Open this publication in new window or tab >>Phonological skills and working memory in children with C1 and Usher typ 1
2012 (English)Conference paper, Poster (with or without abstract) (Refereed)
Abstract [sv]

Bakgrund: Ushers syndrom (USH) innebär hörselnedsättning/dövhet i kombination med Retinitis Pigmentosa och, i två av de tre kliniska typer som finns, ingen eller gradvis förlust av balansfunktion. Det är den vanligaste orsaken till dövblindhet och har varit i fokus i många studier med molekylära, fysiologiska och funktionella konsekvenser av de genetiska mutationerna. Det finns dock få studier med inriktning mot kognitiva aspekter. Föreliggande studie har undersökt kognition med tydlig koppling till hörsel och talspråk hos barn med Ushers syndrom typ 1 och cochleaimplantat.

Metod: Sju barn i åldrarna 7.5-16 år, med bekräftad USH1-diagnos och CI, deltog i studien. Deltagarnas prestation på 10 test, riktade mot fonologiska och lexikala färdigheter samt arbetsminne, jämfördes mot tre kontrollgrupper: barn med normal hörsel, barn med hörselnedsättning och hörapparat, samt barn med icke-syndromal dövhet och cochleaimplantat.

Resultat och slutsats: Liksom i tidigare studier av barn med CI når gruppen med USH1 och CI inte samma nivå avseende fonologiska och lexikala färdigheter, samt presterar signifikant lägre avseende fonologiskt arbetsminne än barn med normal hörsel. Resultaten från föreliggande studie visar dock att deltagarna med USH1 generellt har högre prestationsnivå än andra barn med CI, och presterar på en liknande nivå som barn med hörselnedsättning och hörapparat.

National Category
Social Sciences Interdisciplinary Psychology
Identifiers
urn:nbn:se:liu:diva-78060 (URN)
Conference
Tema Hörsel, March 28-30, Linköping, Sweden
Available from: 2012-06-05 Created: 2012-06-05 Last updated: 2018-01-12
Henricson, C., Lyxell, B., Möller, C. & Lidestam, B. (2012). Phonological skills and working memory in children with Usher type 1 and C1. In: : . Paper presented at ADBN-network meeting, Lund 7-10 November, Sweden.
Open this publication in new window or tab >>Phonological skills and working memory in children with Usher type 1 and C1
2012 (English)Conference paper, Oral presentation with published abstract (Refereed)
National Category
Social Sciences
Identifiers
urn:nbn:se:liu:diva-105061 (URN)
Conference
ADBN-network meeting, Lund 7-10 November, Sweden
Available from: 2014-03-06 Created: 2014-03-06 Last updated: 2014-03-06
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