Junior Research Group »WBS in Resonance«
2. Obergeschoss
Williams Syndrome
Williams Syndrome (WS) is a rare neurodevelopmental disorder caused by a deletion of ~26 genes on chromosome 7q11.23 (Hillier et al., 2003), which occurs in 1 of 7,500 live births (Strømme, Bjørnstad, & Ramstad, 2002). The WS phenotype is typically associated with moderate intellectual disability, specific “elfin” facial structure and physical anomalies cardiac problems, hyper social behavior, anxieties, and a need for lifelong support (Pober, 2010, Royston, Waite & Howlin, 2019). The WS belongs to the group of rare diseases (according to the European Union if less than five out of 10,000 people are affected).
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Current research focuses mainly on clinical characteristics, thus providing important implications for medical management. Parents, therapists and professional caregivers are able to find very few usable implications for everyday-life challenges though.
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The junior research group »WBS in Resonance« was founded in 2016 by Ingolf Prosetzky and Vera Danielsmeier at the HSZG. The term "resonance" stands for an intersubjective "attunement" that is a central aspect of experience for individuals with WS (Prosetzky, 2014). The core group consists of students from the Bachelor's course in Special needs education/Inclusion studies.

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The focus of our work is the evaluation of current international research publications, the development of non-medical theoretical and empirical research approaches, the writing of qualifying theses, global networking with other researchers and the implementation of regional theory-practice transfer projects. The long-term goal is the establishment of a pedagogical competence and advice centre for WS in Görlitz.
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There is close cooperation with the National German WS-Association. Prof. Prosetzky has been a member of the association's scientific advisory board since 2016. An exchange takes place via the association journal, regional, nationwide and international meetings.

- Doctoral thesis Vera Danielsmeier "Herausforderungen, Chancen und Ziele von Personen mit Williams-Beuren-Syndrom – Eine Erfahrungs- und Bedarfsanalyse für zugeschnittene Unterstützungsangebote" (Cooperative Promotion between HSZG, Universität Bremen und Jacobs University Bremen)
- Development of new WS educational guidelines for teachers and parents
- Development, programming and design of two apps to support children and adolescents with the WS (02/2020-12/021)
- Project lead: Prof. Dr. Ingolf Prosetzky and Thomas Dubiel (www.kruemelkiste-app.de), stud. assistants: Sonja Jähnig, Martin Stekkler
- Project partner: Williams-Beuren-Syndrom Bundesverband e.V., Prof. Dr. Matthias Längrich and students from Faculty of Electrical Engineering and Computer Science
- Funding: AOK PLUS - Die Gesundheitskasse für Sachsen und Thüringen
- II. WS Regional Conference/Family meeting at the HSZG, 10.-11. May 2019 in Görlitz: „ My friend must be a heating!“ – Friendship, Loneliness and Social Vulnerability (Engl. Program)
- I.WS Regional Conference/Family meeting at the HSZG, 20.-22. April 2018 in Görlitz
- Danielsmeier, V.; Prosetzky, I. (2018): WBS-Familientreffen und Fachtagung an der Hochschule Zittau/Görlitz. In: Wir üBerunS/Umschau. Zeitschrift des Bundesverbandes WBS. Heft 46, S.78-79.
- Danielsmeier, V. (2018): „Ich sehe was, das Du nicht siehst“. Welche Rolle spielen Emotionen bei der Fähigkeit die Perspektive Anderer einzunehmen? In: Wir üBer unS/Umschau. Zeitschrift des Bundesverbandes WBS. Heft 46, S.37-39.
- Danielsmeier, V. (2017): Towards a tailored support for Williams Syndrome. Learning from individual everyday life experience A holistic multiperspective Mixed Methods study. International Meeting on Williams-Beuren Syndrome "Building our Future". 10.-11.11.2017, Genral Hospital La Paz Madrid (Poster).
- Danielsmeier, V. (2017): Understanding Auditory Aversions in Williams Syndrome. A Longitudinal Mixed Methods Approach. International Meeting on Williams-Beuren Syndrome "Building our Future". 10.-11.11.2017, Genral Hospital La Paz Madrid (Poster).
- Danielsmeier, V. (2017): Wie erleben Personen mit Williams-Beuren-Syndrom Ängste gegenüber Geräuschen? 13. Berliner Methodentreffen Qualitatve Forschung, 21.-22.07.2017, Freie Universität Berlin (Poster).
2020
- Jähnig, S. (2020) Conception of an APP for the prevention of social violence against people with Williams Syndrome. HSZG. Unveröff. Bachelor-Thesis.
2019
- Hölzel, C. (2019): "And the world already looks different for us!" A qualitative study about what mothers and fathers have learned from their child with Williams Syndrome. (in German) HSZG. Unpublished Bachelor-Thesis.
- Siegert, A. (2019): Quality of life for people with intellectual disabilities. Friendship as a "gateway to the world"!? (in German) HSZG. Unpublished Master-Thesis.
- Warschau, I. (2019) "I'm not alone with it!" How do fathers experience and manage the diagnosis of WBS in their child?" (in German) HSZG. Unpublished Bachelor-Thesis.
2018
- Huppe, S. (2018): The personality of individuals with the WBS from the perspective of professional companions in an open description. (in German) Universität Bremen. Unpublished Master-Thesis.
- Köhncke, L. (2018): The self-image of people with WS from the perspective of professional companions. (in German) Universität Bremen. Unpublished Master-Thesis.
- Köster, T. P. (2018): The challenges and opportunities of pedagogical work with people who live under the conditions of WS - Interviews with caregivers. (in German) Universität Bremen. Unpublished Master-Thesis.
2017
- Pestrup, M. (2017): What coping strategies are used by individuals living under the conditions of WS? An exploration study from the perspective of professional companions. (in German) Universität Bremen. Unpublished Master-Thesis.
- Wrieden, A. (2017): To understand stresses in the context of adolescence of individuals who live under the conditions of WS - Advice from the perspective of professional companions. (in German) Universität Bremen. Unpublished Master-Thesis.
Hillier, L. W., Fulton, R. S., Fulton, L. A., Graves, T. A., Pepin, K. H., Wagner-McPherson, C., ... & Minx, P. (2003). The DNA sequence of human chromosome 7. Nature, 424(6945), 157-16
Pober, B. R. (2010). Medical progress: Williams-Beuren syndrome. New England Journal of Medicine, 362(3), 239-252. doi:10.1056/NEJMra0903074
Prosetzky, I. (2014). Mehr als die Summe seiner Symptome: Zur kulturhistorischen Neuropsychologie und Pädagogik des Williams-Beuren-Syndroms. Schriftenreihe International Cultural-historical Human Sciences: Vol. 48. Berlin: Lehmanns.
Royston, R., Waite, J., & Howlin, P. (2019). Williams syndrome: recent advances in our understanding of cognitive, social and psychological functioning. Curr Opin Psychiatry, 32(2), 60-66. doi:10.1097/YCO.0000000000000477
Strømme, P., Bjømstad, P. G., & Ramstad, K. (2002). Prevalence estimation of Williams syndrome. Journal of child neurology, 17(4), 269-271.