1. Javad Jamshidi Fasa University of Medical Sciences, November 2014 Session 5 Medical Genetics Patterns of Inheritance Part 2

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3. 3 Affected females are more frequent than affected males All daughters of a affected male, will be affected Females are usually less severely affected than males

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6. 6 The trait or disorder should affect males almost exclusively Are transmitted through unaffected carrier females to their sons Male-to-male transmission is not observed Daughters of affected males are obligate carriers

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8. 8 Occurs at around 15 to 16 days' gestation, when the embryo consists of approximately 5000 cells Normally either of the two X chromosomes can be inactivated in any particular cell. Thereafter the same X chromosome is inactivated in all daughter cells The inactive X chromosome exists in a condensed form during interphase (bar body)

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11. 11 Images from: Emery's Elements of Medical Genetics, 14th Edition, by Peter D. Turnpenny and Sian Ellard, (2012)

12. 12 Occasionally a woman might manifest features of an X- linked recessive trait. Homozygosity for X-Linked Recessive Disorders Skewed X-Inactivation Numerical X-Chromosome Abnormalities X-Autosome Translocations

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14. 14 Only males are affected. An affected male transmits Y-linked traits to all of his sons but to none of his daughters.

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17. 17 Autosomal traits that express more frequently in one sex than in another Gout and presenile baldness Hemochromatosis

18. 18 In some autosomal dominant disorders, the onset of the disease occurs at an earlier age in the offspring or occurs with increasing severity A result of the expansion of unstable triplet repeat sequences Huntington disease and myotonic dystrophy

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21. 21 Each cell contains thousands of copies of mitochondrial DNA Mitochondrial DNA has a higher rate of spontaneous mutation than nuclear DNA Mitochondria, and therefore their DNA, are inherited almost exclusively from the mother A number of rare disorders with unusual combinations of neurological and myopathic features

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