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Clinical Genetics

Clinical Genetics. Renata Gaillyová. Clinical Genetics. schoolroom, University Hospital Brno, Children's Hospital Brno, Černopolní 22 Monday 8:00–12:30 Clinical Genetics Tuesday 8 :00-10:30 DNA Diagnostics

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Clinical Genetics

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  1. Clinical Genetics Renata Gaillyová

  2. Clinical Genetics • schoolroom, University Hospital Brno, Children's Hospital Brno, Černopolní 22 • Monday 8:00–12:30 Clinical Genetics • Tuesday 8:00-10:30 DNA Diagnostics 10:00-12:30 Visit on the Department of Medical Genetics (Children's Hospital, Černopolní 9, Building G, 3th floor) Bring a medical mantle and shoes in the laboratory, please use the changing rooms for students • Wednesday 8:00 - 10:00 Clinical Cytogenetics • Writing test – terms are in IS

  3. Clinical genetics • Dept. of medical genetics • Genetic prevention • Genetic diseases • Patients on the departement of clinical genetics • Genetic counselling • Chromosome abnormalities • AD,AR,XR inheritance, disorders • Multifactorial inheritance • Teratogenes, Environmental hazards • Prenatal diagnosis • Reproductive genetics • Hereditary cancer

  4. Dept. of Medical genetics • Genetic ambulance genetic counselling • Laboratory part • Cytogenetic laboratories Prenatal cytogenetics Postnatal cytogenetics Oncocytogenetics Molecular – cytogenetics • Lab. for DNA and RNA analysis (clinical genetics and oncogenetics)

  5. Characteristic of Medical Genetics • Preventive Medicine • Interdisciplinary cooperation • Information from genetics (disease, posibilities of testing, prenatal analysis) • Voluntary choice for patients • Informed agreement

  6. Primary genetic prevention • Before pregnancy • Folic acid (cca 0,8 mg/day, 3+3 months) • Vaccination (rubella) • Genetic counselling • Contraception, family can opt for adoption or donor of gamets (oocytes, sperm) • Pregnancy planning • Rediction of environmental hazards (drugs, radiation, chemicals…)

  7. Reproduction of the optimal age In women increases the risk of accidental congenital chromosomal aberrations in the offspring In men may increase the risk of de novo mutations in some monogenic diseases (Neurofibromatosis I, Achondroplasia..)

  8. Prevention of spontaneous and induced mutations Healthy Lifestyle The restriction of harmful substances - drugs, environmental hazards

  9. Vacctination, infection prevention Prevention of rubella embryopathie Prevention of congenital toxoplasmosis Testing for infectious disease risk in mothers (CMV, varicella-zoster virus, ...)

  10. Vitamin prevention of neural tube defects, anterior abdominal wall defects, clefts Folic acid at a dose of 0.8 mg daily (twice the dose in non-pregnant) for 3-6 months prior to conception and till the end of 12. week of pregnancy

  11. Examination of acquiredchromosomal aberrations Preventive examinations of persons exposed to environmetal risksat work or persons with risk of long-term therapy (immunosuppressants, cytostatics, ....) The possibility of vitamin therapy to improve repair of DNA (3-6 months)

  12. Contraception, sterilization Contraception - temporarily prevents conception in the limited impact of risk (treatment) Sterilization - the long-term inhibition of pregnancy in a high risk of disease in the offspring (Hereditary disease)

  13. Adoption Alternative family care as an option at high genetic risk families

  14. Donation of sperm, oocytes and embryos reduction in high genetic risk reproductive problems

  15. Secondary genetic prevention • Prenatal diagnosis • Prenatal screening • Prenatal tests • Genetic counselling • Termination of pregnancy (the law in Czech Republic- end of 24. week of gestation) • Postnatal screening • Newborn screening

  16. Genetics diseases • Chromosome abnormalities • about 0,6 - 0,7% • Monogen diseases • about 0,36% (study in 1 000 000 newborns) • most then 90% of monogen diseases occur in childhood • Multifactorial (polygenic or complex) disorders • Occur in about 80% in the population

  17. Patients on genetic departements • Dead person • Adults • Pregnant women • Fetuses • Children

  18. Patients on genetic departements • Positive family history (chromosome abnormality, congenital malformations, mental retardation, diseases…) • Pregnant women with encrease risk for the fetus • Infertility – sterility, repeated fetal loss • Donors (gamets) • Patients with tumours

  19. Children • Congenital malformations

  20. Children • Suspition of mongenic hereditary diseases or inherited metabolic disorders and their families

  21. Children • Suspition on congenital chromosom aberations (children with congenital malformations, abnormal face, atipical visage, pre- or postnatal growth retardation, premature birth)

  22. Children • early or delayed puberty • Malformations of the external or internal genitalia • Low or high figure

  23. Children • Preventiv genetic examinatioun before adoption

  24. Children or adults • Mental retardation • Psychomotor retardation • Developmental delay

  25. Children and adults • Gender identity disorder

  26. Children and adults • people with long-term exposure to environmental pollutants • (alcohol, cigarettes, drugs, radiation)

  27. Children and adulds • patients with suspected hereditary cancer • patients with cancer (sporadic occurrence)

  28. Adults • Donors of gametes (preventive tests)

  29. Adults • Related partners (increased risk for hereditary disease with AR inheritance)

  30. adults • Infertility • Repeated spontaneous abortions

  31. Pregnant women • With unfavorable family history

  32. Pregnant women • with adverse pregnancy history (chronic diseases with established therapies, acute disease in early pregnancy - temperature, drugs, X-rays, CT, vaccinations, toxoplasmosis, rubella, ...)

  33. Pregnant women • Prenatal biochemical screening (Pathological results)

  34. Pregnant women • Ultrasound prenatal screening – pathological results • Congenital malformations in the fetus • Risk of chromosomal abnormality in the fetus

  35. Genetic counselling • Anamnesis • Family history • Pedigree analysis • Examination of the patient • Laboratory analysis • Other examinations - neurology, psychology, hematology, CT, MRI …

  36. Three-generation pedigree • Patient • Siblings • Children siblings • Parents • Parents siblings • Children of parents siblings • Parents parents

  37. man marriage woman divorce Unknown gender konsanguinity diseased monozyg. twins dizygot. twins carrier childless proband miscarriage dead person

  38. Clinical examination

  39. Next steps • Recommend the laboratory genetic testing • Recommend other specialists if needed • Require medical records • Make photodocumentation

  40. The result of genetic counselling • Specify exact diagnosis (if possible) • Determine genetic prognosis • Is the disease hereditary? • Type of inheritance • Genetic risks for other family members • Posibilities of treatment, prenatal analysis

  41. Man Cell Chromosome DNA Man

  42. Chromosome abnormalities 0,6-0,7% live born

  43. Congenital chromosome abnormalities • Autosomes • Gonosomes • Numerous • Structural • Balanced • Unbalanced

  44. Populations frequency

  45. G-pruhy

  46. Chromosome abnormalities in spont. abortions

  47. Maternal age and chromosome abnormalities in AMC (per 1000)

  48. Risk of Down syndrom(live births)

  49. Down syndrome

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