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The examination builds upon the previous instruction in propedeutics and pediatrics. It focuses on the etiology, pathophysiology, symptomatology, diagnosis, differential diagnosis, and treatment of age-specific diseases. The examination includes a practical part—examination, diagnosis, and treatment proposal for a specific patient. The theoretical part of the exam also includes a question from clinical genetics.
Last update: David Jan, doc. MUDr., Ph.D. (21.05.2025)
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The objective is to complete pediatric education for 6th-year students to the extent required for the state final exam and the graduate profile.
Last update: David Jan, doc. MUDr., Ph.D. (21.05.2025)
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Marcdante KJ, Kliegman RM. Nelson Essentials of Pediatrics. Elsevier, 2018. Bláhová K, Fencl F, Lebl J, et al. Pediatrická propedeutika. Galén, 2019. David J, Votava F, et al. Diferenciální diagnostika vybraných pediatrických stavů. Grada, 2025. Janota J, Straňák Z, et al. Neonatologie. EEZY, 2023. Lebl J, Janda J, Pohunek P, Starý J, et al. Klinická pediatrie. Galén, 2014. Mixa V, Heinige P, Vobruba V, et al. Dětská přednemocniční a urgentní péče. Grada, 2024. Muntau AC. Pediatrie. Grada, 2014. Last update: David Jan, doc. MUDr., Ph.D. (21.05.2025)
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Part of state examination in pediatrics. Last update: David Jan, doc. MUDr., Ph.D. (21.05.2025)
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State examination in pediatrics. Questions for the state exam in pediatrics (from 2025/2026):
Questions from Clinical Genetics for 6th Year – State Examination from Pediatrics (from 2025/2026):
1. Reproduction genetics, preconception genetic testing 2. Preimplantation genetic testing – indications, types and techniques 3. Noninvasive screening in the 1st and in the 2nd trimester of pregnancy 4. Invasive prenatal diagnostics in the 1st and in the 2nd trimester of pregnancy 5. Postnatal (newborn) screening and predictive (presymptomatic) testing 6. Teratogenic factors and congenital abnormalities, risk groups of pharmaceuticals 7. Cytogenetic examinations of chromosomal abnormalities 8. Molecular genetic examinations of monogennic diseases 9. Multifactorial diseases – risk calculation, genetic testing, significance of epigenom 10. Possibilities of therapy of genetic diseases, including gene therapy 11. Syndromes associated with numerical abnormalities of chromosomes 12. Syndromes associated with structural aberrations of chromosomes, also microdeletion 13. Syndromes of chromosomal instability 14. Hereditary tumour diseases, diagnostics, possibilities of prevention 15. Molecular changes in neoplasia – at the level of chromosomes and DNA 16. Genetic causes of mental retardation, diagnostics 17. Genetic causes of immunity disorders, monogenic and polygenic, within syndromes 18. Genetic examinations in cardiology, diagnostics, examples of diseases 19. Monogenic diseases affecting the nervous system 20. Monogenic diseases affecting the endocrine system 21. Monogenic diseases affecting haematopoesis and haemocoagulation 22. Monogenic diseases affecting the sense organs 23. Monogenic diseases affecting the connective tissue 24. Monogenic diseases affecting the skin 25. Monogenic diseases affecting the muscles 26. Monogenic diseases affecting the skeletal system 27. Diseases associated with expansion of repetitive sequences 28. Gene imprinting and associated syndromes 29. Lysosomal storage disorders and mitochondrial diseases 30. Familial hypercholesterolemia and Smith-Lemli-Opitz syndrome Last update: David Jan, doc. MUDr., Ph.D. (02.10.2025)
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Review of physical examination of neonates, infants, toddlers, preschool and school-aged children, and adolescents; pediatric medical history. Interpretation of laboratory and imaging methods in pediatrics. Special emphasis is placed on: neonatology, pneumology, allergology and immunology, rheumatology, gastroenterology, endocrinology and diabetology, hematology and oncology, nephrology, clinical genetics, clinical nutrition and metabolic disorders, intensive care and resuscitation; and primary pediatric care.
Last update: David Jan, doc. MUDr., Ph.D. (21.05.2025)
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