Prof. Dr. phil. Ingolf Prosetzky

Photo: Prof. Dr. phil. Ingolf Prosetzky
Heilpädagogik/Inclusion Studies
Prof. Dr. phil.
Ingolf Prosetzky
Faculty of Social Sciences
02826 Görlitz
Furtstrasse 2
Building I, Room 2.07
2nd upper floor
+49 3581 374-4287

Website: Researchgate

Professorship

Heilpädagogik / Inclusion Studies

  • Selected publications

    Prosetzky, I. (2024): Interaction of loneliness with chronic illnesses and disabilities - with a special focus on conditions of mental disability. Expertise 09 for the Loneliness Competence Network.

    Silter, K.; Hilkenmeier, J.; Beck, I.; Franke, N.; Prosetzky, I. (2023): Perceived burdens and resources of people with and without disabilities during the first COVID-19-related lockdown in Germany: First results of an international survey. Journal for Inclusion,  3. 

    Sideropoulos, V.; Van Herwegen, J.; Meuleman, B.; ... Prosetzky, I. ...; Samson, A.C. (2023): Anxiety, concerns and COVID-19: Cross-country perspectives from families and individuals with neurodevelopmental conditions. Journal of Global Health 13:0408. DOI: 10.7189/jogh.13.04081

    Prosetzky, I. (2019): The category 'friendship' in cultural-historical theory - suggestions for/by researching the Williams-Beuren syndrome?! In: Yearbook of the Luria Society 2019, 61-91, ISBN: 978-3-96543-081-5

    Prosetzky, I. (2019): Report from the visit to the WSA National Convention 2018 in the USA. In: Wir üBer unS/Umschau. Journal of the Federal Association WBS. Issue 47, 54-57.

    Prosetzky, I., Danielsmeier, V. (2018): Buildung a Competence Center for Wiliams Syndrome at the Hochschule Zittau/Görlitz - Current Research, Teaching and Third Mission. ACC Journal, Vol. 24, Issue 3, DOI: 10.15240/tul/004/2018-3-010

    Prosetzky, I.  (2017): University didactic reflections on the (in)compatibility of diagnostics and inclusion. In: Römer, S. (ed.): Diagnostics as relationship design. Entering into, reflecting on and shaping relationships - diagnostics in dialog and cooperation. Berlin, Frank & Timme, 81-124.

    Prosetzky, I. (2014): More than the sum of its symptoms: On the cultural-historical neuropsychology and pedagogy of Williams-Beuren syndrome. Berlin: Lehmanns Media. Publication series International Cultural-historical Human Sciences. Volume 48.

    Prosetzky, I. (2013): General developmental levels and domain specificity. In: G. Feuser; J. Kutscher & B. Siebert (Eds.): Development and Learning. Vol. 7 of the Encyclopaedic Handbook of Disability Education "Disability, Education and Participation". Stuttgart: Kohlhammer, 103-114.

    Prosetzky, I. (2009): Isolation and participation. In: M. Dederich & W. Jantzen (ed.): Behinderung und Anerkennung. Vol. 2 of the Encyclopaedic Handbook of Disability Education "Disability, Education and Participation". Stuttgart: Kohlhammer, 87-95.

  • Committees/memberships

    Institute for Transformation, Housing and Social Spatial Development (TRAWOS)

    WS-iReach research network

    Scientific Advisory Board of the Williams-Beuren Syndrome Federal Association e.V.

    German Interdisciplinary Society for the Promotion of Research for People with Intellectual Disabilities e. V.

    Luria Society. Association for the promotion of the scientific foundation and rehabilitation of brain-damaged people e.V.

  • Professional career

    since 2015 Professor at the Faculty of Social Sciences, Zittau/Görlitz University of Applied Sciences

    2014-15 Lecturer in the Department of Inclusive Education, University of Bremen

    2007-14 Specialist for psychological counseling and diagnostics at Elbe-Werkstätten GmbH/Nord, Hamburg

Photo: Prof. Dr. phil. Ingolf Prosetzky
Heilpädagogik / Inclusion Studies
Prof. Dr. phil.
Ingolf Prosetzky
Faculty of Social Sciences
02826 Görlitz
Furtstrasse 2
Building I, Room 2.07
2nd upper floor
+49 3581 374-4287

Website: Researchgate

Research focuses
  • Pedagogical and everyday life relevant knowledge about Williams(-Beuren)-Syndrome
  • Participation und Participative research
  • Rehistorisierung and Cultural-historical Human Sciences

Research and knowledge transfer projects about 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 WSS belongs to the group of rare diseases (according to the European Union if less than five out of 10,000 people are affected).

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.

Other Research and knowledge transfer projects

Research and knowledge transfer projects on Williams-Beuren syndrome (WBS)

Williams-Beuren syndrome (WBS) is a rare neurodevelopmental impairment that is often associated with mental retardation, heart defects, a special facial structure ("elfin face"), hypersocial behavior, anxiety and lifelong support needs (Pober, 2010, Royston, Waite & Howlin, 2019). It is based on a randomly occurring deletion of around 26 genes on chromosome 7q11.23 (Hillier et al., 2003). The prevalence is 1:7,500 (Strømme, Bjørnstad, & Ramstad, 2002). WBS belongs to the group of rare diseases (according to the European Union, when fewer than five in 10,000 people are affected).

The genetic, neurobiological and medical basis of WBS is now relatively well researched, but there is a lack of educational knowledge relevant to everyday life, which would be extremely helpful for people with WBS, their relatives and professional caregivers.

Other research and knowledge transfer projects