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Autor: Jan Viktorin

In: Studia Scientifica Facultatis Paedagogicae Universitas Catholica Ružomberok

ISSN: 1336-2232

Ročník: XXIV.

Číslo: 2

Strany: 65-77

Rok vydania: 2025

Vydavateľ: VERBUM – vydavateľstvo Katolíckej univerzity v Ružomberku

Abstract: The paper deals with the specifics of a person with a rare genetic disorder called Prader-Willi syndrome. It presents the results of qualitative research in the form of a case study of a person with Prader-Willi syndrome. The aim of the paper is to describe the educational opportunities of a person with Prader-Willi syndrome and the extent to which a person with Prader-Willi syndrome influences the functioning of the family. The results of the research show that a person with Prader-Willi syndrome currently has a relatively wide range of educational opportunities, from kindergartens, through primary schools to secondary schools. The birth of a person with Prader-Willi syndrome significantly interferes with the functioning of the family and also has a fundamental impact on the further functioning of the family.

Keywords: Prader-Willi syndrome. Symptoms. Disorder of intellectual development. Communication. Family. Education.

Citácia:

VIKTORIN, Jan, 2025. Osoba s Prader-Williho syndrómom. In: Studia Scientifica Facultatis Paedagogicae Universitas Catholica Ružomberok. Online. Ružomberok: VERBUM – vydavateľstvo Katolíckej univerzity v Ružomberku, roč. XXIV., č. 2, s. 65-77. ISSN 1336-2232. Dostupné na: