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Beyond Mendel

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Down Syndrome Trisomy 21 ... Down Syndrome: 1 in 700 children will have an extra chromosome 21. Trisomy 21. Karyotype of a Female with Down Syndrome. Down ... – PowerPoint PPT presentation

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Title: Beyond Mendel


1
Beyond Mendel
2
Beyond Mendel
  • Some genetic disorders do not follow simple
    Mendelian transmission.
  • They do not seem to run in families
  • Many of these disorders are caused by changes in
    chromosome number aneuploidy.
  • Aneuploidy can result from changes in autosomal
    count or the number of sex chromosomes.
  • XO
  • XXX
  • XXY
  • XYY

3
Alterations of Chromosomal Number or Structure
  • How do alterations in chromosomal number occur?
  • Nondisjunction Errors during Meiosis.
  • Homologous chromosomes do not separate during
    Meiosis I
  • Sister chromatids do not separate during Meiosis
    II.

4
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5
Down Syndrome Trisomy 21
  • Most zygotes containing chromosomal alterations
    are spontaneously aborted.
  • However, some aneuploid conditions are viable.
  • Down Syndrome 1 in 700 children will have an
    extra chromosome 21. Trisomy 21

6
Karyotype of a Female with Down Syndrome
7
Down Syndrome
  • Symptoms include
  • Syndrome typical facial features
  • Short stature
  • Heart defects
  • Life expectancy 17 yrs
  • Mental retardation due to CNS malformations
  • Reduced neuron count Low brain weight
  • Reduced depth of sulci
  • Shorter than normal dendrites
  • I.Q. 20 50

8
Incidence of D.S. correlated with maternal age
  • Before birth, all human female gametes are
    arrested during late prophase I when homologous
    chromosomes are in Tetrads.
  • Only a single gamete completes Meiosis during
    each menstrual cycle.
  • The older the female, the longer the gametes have
    been sitting in prophase I.

9
Tuner Syndrome XO
  • Affected people lack a second sex chromosome.
  • Sexed as girls at birth.
  • Ovaries do not produce estrogens. Must be treated
    during adolescence to induce puberty.
  • Other symptoms include
  • Short stature
  • Syndrome typical facial features
  • Sterile
  • Heart defects
  • Webbing of skin on the neck
  • Lack of secondary sex characteristics if not
    treated

10
Turner Syndrome
  • Overall intelligence is normal
  • Specific disabilities in map reading and spatial
    orientation tasks.
  • Dreams are deficient in visual imagery and
    resemble those of blind people.

11
Turner Syndrome XO
12
Klinefelters Syndrome XXY
  • Individuals posses an extra X chromosome. 1 in
    600 births
  • Presence of TDF allows masculinization sexed as
    males at birth
  • Symptoms
  • Tall
  • Slightly feminized physique
  • Poor beard growth
  • Breast development
  • Testicular atrophy
  • Sterile
  • Mental retardation

13
Superman XYY
  • Extra Y chromosome 1 in 850 births
  • May be sterile
  • Symptoms
  • Very tall
  • Mental retardation
  • Exaggerated male secondary sex characteristics

14
XYY
  • During the seventies the XYY genotype was
    believed to promote aggressive, antisocial
    behaviors.
  • A disproportionably large number of XYY
    individuals were incarcerated.
  • Measures of aggression showed no correlation
    between XYY genotype and increased aggression.
    Third variable?
  • Less intelligent than average
  • Much Taller than average
  • Crimes committed were most often non-violent

15
XYY
  • XYY males less likely to establish good
    relationships with women, less likely to marry.

16
XXY and XYY Males
17
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