SubjectsSubjects(version: 825)
Course, academic year 2014/2015
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State Examination in Paediatrics - CPADXX36R
Czech title: Dětské lékařství
Guaranteed by: Deparment of Children and Adolescents (12-KDD)
Faculty: Third Faculty of Medicine
Actual: from 2014
Semester: both
Points: 0
E-Credits: 0
Examination process:
Hours per week, examination: 0/0 STEX [hours/week]
Capacity: winter:unknown / unknown (unknown)
summer:unknown / unknown (unknown)
Min. number of students: unlimited
State of the course: taught
Language: Czech, English
Teaching methods: full-time
Level:  
Note: deregister from the exam date if a requisite was not fulfilled
you can enroll for the course in winter and in summer semester
Guarantor: doc. MUDr. Felix Votava, Ph.D.
Classification: Medicine > Clinical Disciplines
Annotation -
Last update: Eva Mattušová (26.05.2008)

State rigorous examination in pediatrics
Aim of the course -
Last update: Mgr. Alena Vlasáková, DiS. (19.11.2008)

Part of SE

Literature -
Last update: Eva Mattušová (21.10.2008)

Nelson Essentials of Pediatrics, E.Behrman, RM Kliegman, Saunders 2007

Teaching methods -
Last update: Mgr. Alena Vlasáková, DiS. (19.11.2008)

Part of SE

Requirements to the exam -
Last update: Sylvie Zadražilová (09.11.2017)

State rigorous examination in pediatrics

Questions for the examination in pediatrics from 2016/2017:

 

 

General pediatric problems, neonatology,

congenital defects

Diseases

Differential Diagnosis  of Symptoms

1.       

Different childhood periods and their main characteristics

Disorders of the esophagus and of the stomach

Fever   

2.       

Growth  and its evaluation, growth charts

Diarrhoea – dehydration and rehydration

Exanthema 

3.       

Breastfeeding and its importance

Liver diseases,  portal hypertension

Headache  

4.       

Formula feeding in infants and types of formulas

Disorders of the adrenal glands

Seizure, tetany (apart from newborn)

5.       

Preventive care in pediatrics, regular check-ups

Disorders of the intestine (apart from autoimmune)

Polyuria-polydipsia

6.       

Vaccination

Calcium-phosphate metabolism disorders

Meningeal irritation

7.       

Psychomotor development and its evaluation

Anaphylactic shock

Hematuria

8.       

Growth charts

Inherited disorders of metabolism with acute decompensation in neonatal and infant period

Abdominal pain

9.       

Water soluble vitamins and trace elements

Hypercholesterolemia and dyslipidemias in children

Heart rhythm disorders in children

10.     

Puberty - its evaluation and disorders

Inherited metabolic disorders with chronic course

Enlarged lymph nodes

11.     

Injuries and intoxications in children

Diabetes mellitus and diabetic ketoacidosis

Failure to thrive and weight-loss

12.     

Problematics of foreign bodies in children

Streptococcal and staphylococcal infections

Edema

13.     

Problems related to adolescence

Infections of the central nervous system

Vomiting 

14.     

Social aspects in pediatrics, child abuse and neglect syndrome

Vasculitis  (Henoch-Schönlein purpura, Kawasaki disease)

Large abdomen

15.     

Water balance related to age, dehydration

Tuberculosis

Arterial hypertension

16.     

Nutrition and eating disorders

Chronic kidney diseases

Hyper/ hyponatremia, hyper/ hypokalemia

17.     

Fat soluble vitamins

Autoimmune diseases (apart from vasculitis)

Delayed and precocious puberty

18.     

Minerals and their disorders

Herpetic infections

Anuria, oliguria

19.     

Parenteral and enteral nutrition

Urinary tract infections

Exspiratory dyspnea

20.     

Shock  in pediatrics

Cystic fibrosis

Obesity

21.     

Neurotic and behavioral disorders

Periodic fever

Hypoglycemia

22.     

Disorders of acid-base balance

Inborn and acquired anemias

Hepatomegaly and  splenomegaly

23.     

Pharmacotherapy in pediatrics

Nephrotic syndrome

Psychomotor retardation

24.     

Characteristics of a newborn, postnatal adaptation

Laryngitis and epiglotitis

Joint pain, gait disorders

25.     

Cardiopulmonary resuscitation in children

Lower respiratory tract disorders

Proteinuria

26.     

Prematurity and its complications

Oncological diseases in children (apart from hemoblastoses)

Enuresis, voiding disorders

27.     

Newborn screening

Heart diseases ( apart from congenital heart defects )

Changes in white blood cell count

28.     

Life threatening congenital developmental defects

Platelet disorders

Inspiratory dyspnea and stridor

29.     

Respiratory disorders in  newborns, perinatal hypoxia

Hemoblastoses in children

Blood protein disorders

30.     

Neonatal jaundice, newborn hemolytic disease

Thrombophilic conditions

Cough

31.     

Neonatal infections, congenital infections

Blood coagulation disorders

Disturbances of consciousness

32.     

Congenital anomalies of the urinary tract

Allergic diseases in childhood

Jaundice

33.     

Congenital anomalies of the respiratory tract

Disorders of the thyroid gland

Increased sedimentation rate

34.     

Congenital anomalies of the gastrointestinal tract

Bone, muscle and joint disorders in childhood

Cyanosis

35.     

Congenital heart defects without a shunt

Disorders of sexual development / differentiation

Constipation

36.     

Congenital heart defects with shunt lesions

Inflammatory  bowel disease (IBD), celiac disease 

Growth disorders

37.     

Perinatal trauma

Malabsorption syndromes

Micro-  and macrocephaly

38.     

Development and disorders of the immune system

Disorders of neurohypophysis

Acute abdomen – peculiarities in children

39.     

Sudden infant death syndrome, infant mortality rate

Disorders of adenohypophysis

Recurrent respiratory tract infections

40.     

Childhood exanthema diseases

Invasive bacterial infections - sepsis

Diarrhoea

 

Questions for the examination in clinical genetics from 2016/2017:

 

 

 

1.     Prevention of genetic diseases and preconception care

 

2.     Genetic consultation and methods of genetic consultation

 

3.     Screening and prenatal diagnostics in the 1st trimester of pregnancy

 

4.     Screening and prenatal diagnostics in the 2nd trimester of pregnancy

 

5.     Summary of methods of prenatal diagnostics, invasive for the fetus

 

6.     Summary of methods of prenatal diagnostics, non-invasive for the fetus

 

7.     Postnatal screening

 

8.     Indications and methods of prenatal cytogenetic examination

 

9.     Occurrence and classification of genetic diseases

 

10.  Possibilities of therapy of genetic diseases

 

11.  Syndromes associated with numerical abnormalities of autosomes

 

12.  Syndromes associated with structural aberrations of autosomes

 

13.  Syndromes associated with chromosomal abnormalities of gonosomes

 

14.  Microdeletion syndromes

 

15.  Autosomal dominant diseases with manifestation in childhood

 

16.  Autosomal recessive diseases with manifestation in childhood

 

17.  X-linked recessive diseases with manifestation in childhood

 

18.  Cancer diseases of childhood

 

19.  Chromosomal changes in neoplasia

 

20.  Chromosomal instability syndromes

 

21.  Hereditary and familial tumor diseases

 

22.  Preventive arrangement in families with hereditary malignant occurrence

 

23.  Multifactorial heredity, diabetes mellitus and allergies

 

24.  Teratogenic factors and congenital abnormalities, risk groups of pharmaceuticals

 

25.  Heredity of inborn heart defects

 

26.  Genetics of cystic fibrosis

 

27.  Genetics of hypercholesterolemia and atherosclerosis

 

28.  Inborn defects of immunity

 

29.  Monogenic diseases affecting skin

 

30.  Monogenic diseases affecting connective tissue

 

31.  Monogenic diseases affecting haematopoesis

 

32.  Monogenic diseases affecting haemocoagulation

 

33.  Monogenic diseases affecting skeletal system

 

34.  Monogenic diseases affecting nervous system

 

35.  Monogenic diseases affecting muscles

 

36.  Hereditary metabolic diseases

 

37.  Monogenic diseases affecting lysosomes

 

38.  Monogenic hormonal disorders

 

39.  Genetic causes of mental retardation

 

40.  Gene imprinting and associated syndromes

 

 

       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       

 

       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
       
Syllabus -
Last update: Eva Mattušová (21.10.2008)

The repeating of physical examination of newborn, infant, toddler, prescholl and school child and adolescent, the repeating of taking patient´s history, interpretation of some findings and results in pediatrics ? laboratory, X-ray. Special emphasis to respiratory diseases, oncology, neonatology, autoimmunity, immunodeficiency, gastroenterology, diabetology, disorders of homeostasis, endocrinology, hematology, imaging methods, nephrology, thyreology and espacially to differantial diagnostic discussions.

 
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