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Student with developmental dysphasia and specific learning disabilities
Jobánková, Tereza ; Klenková, Jiřina (advisor) ; Květoňová, Lea (referee)
The diploma thesis is focused on the problems and relationship of specific language impairment and learning disabilities, as developmental disorders affecting not only speech and language, but also other areas influencing the educational process and school success of pupils. The introductory chapters are devoted to the theoretical definition of individual disorders with a focus on their terminology, etiology, symptomatology, diagnostics and therapy. Attention is also focused on the reciprocal context of specific language impairment and difficulties in reading, writing and orthography. The thesis is a comparative case study whose aim is to describe and compare the symptoms of the abovementioned disorders in a selected group of pupils of younger school age as reflected in basic school skills - reading and writing. The purpose of the thesis is to point out their interdependence and similarity in the field of education, but also certain specifics of each of the disorders depending on the individual peculiarities of each pupil.
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Cystic fibrosis
Riedrová, Michaela ; Herink, Josef (advisor) ; Semecký, Vladimír (referee)
Bachelor thesis deals with the topic of cystic fibrosis. It is a serious autosomal recessive hereditary disease. Cystic fibrosis can not be cured, it is only possible to treat the complications of this disease. The thesis is divided into the theoretical and practical part. The theoretical part is focused on the occurrence of cystic fibrosis in the world and in the Czech Republic, history, the principle of inheritance of cystic fibrosis and there are presented the symptoms and complications associated with cystic fibrosis. There are also presented diagnostic methods and principles, therapy of the disease. In the practical part of the bachelor thesis there is a public survey on the topic of cystic fibrosis. The survey was conducted in the form of a questionnaire. Key words: cystic fibrosis, mucoviscidosis, CFTR gene, hereditary diseases, chlorides in the sweat
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