Developmental Psy 1

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    Biological Beginnings

    Module 2

    Part 1- GeneticFoundations

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    The genetic process

    Cell

    Nucleus

    Chromosomes

    DNA

    Genes

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    Chromosomes

    Threadlike structuresthat contain thegenetic substanceDNA.

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    DNA (Deoxyribonucleic

    acid)

    A complex moleculethat contains geneticinformation.

    Within cells, DNA isorganized into X-shaped structurescalled chromosomes

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    Genes

    Units ofhereditaryinformation composed ofDNA. Genes direct cells to

    reproduce themselves andmanufacture the proteinsthat maintain life

    A gene is the basic unit of

    heredity in a living organism.

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    Genome

    The complete set ofdevelopmental instructions forcreating proteins that initiatethe making of a humanorganism.

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    Mitosis

    Cellular reproduction inwhich the cells nucleus

    duplicates itself with twonew cells being formed,each containing the sameDNA as the parent cell,

    arranged in the same 23pairs of chromosomes.

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    Meiosis

    A specialized form of celldivision that occurs to

    form eggs and sperm.

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    Zygote

    A single cell formedthrough fertilization.

    It is the next stage in inthe process of ofreproduction.

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    Sources of variability

    X chromosome and Ychromosome

    Genotype- all of a personsgenetic material.

    Phenotype-the way anindividual genotype isexpressed in observed and

    measurable characteristics.

    Heredity environmentinteraction.

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    Genetic principles

    Dominant recessive genesprinciple

    Sex linked genes

    Genetic imprinting

    Polygenic inheritance

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    Dominant recessive genes principle

    Dominant Inheritance a pattern ofinheritance in which, when a child receivescontradictory alleles, only the dominant one isexpressed.

    Recessive Inheritance a pattern of

    inheritance in which a child receives identicalrecessive alleles, resulting in expression of anon dominant trait.

    Alleles paired genes (alike or different) that

    affect a trait. When bot

    hthe alleles are t

    hesame , the person is is homozygous . When

    they are different the person is heterozygous.

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    Homozygous possessing two identicalalleles for a trait.

    Heterozygous possessing differingalleles for a trait.

    Polygenic inheritance pattern ofinheritance in which multiple genes

    affect a complex trait.

    Multifactorial transmission acombination of genetic andenvironmental factors to produce certaincomplex traits.

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    Chromosomal and gene linkedabnormalities

    Down syndrome trisomy 21.

    Failure of the 21st chromosome toseparate during meiosis. In some cases anextra broken piece of a 21st chromosomeis present.

    Downs syndrome is characterized by-

    Mental retardation.

    Memory and speech problems, limitedvocabulary and slow motor development.

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    Distinct physical features which include-a short stocky build, a flattened nose, a

    protruding tongue, almond shaped eyes,and an unusual crease running acrossthe palm of the hand.

    Others conditions include eye

    cataracts, heart and intestinal defects

    Short lifespan.

    Difficulties in breathing and feeding.

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    Other abnormalities.

    Cooley anemia (R)

    Cystic fibrosis (R)

    Phenylketoneuria (R)

    Sickle cell anemia (R)

    Tay sachs disease (R)

    Huntington disease (D)

    Marfan syndrome (D)

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    Abnormalities related to the

    sex chromosomes

    XYY syndrome extra ychromosome. Above avgheight, large teeth andsometimes severe acne.Intelligence male sexualdevelopment and fertilityare normal

    1 in 1000 male birthsNo special treatment isnecessary.

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    Triple X syndrome- extra

    X chromosome . Tallnessand impaired verbalintelligence. Female sexual

    development and fertilityare normal.

    1in 500 to 1250 female

    births

    Special edu to treat verbaland ability problems.

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    Klienfelter syndromeXXY extra Xchromosome. Tallness, body

    fat distributing females,incomplete development ofsex characteristics atpuberty, sterility, andimpaired verbal intelligence.

    1 in 900 male births .

    Hormone therapy atpuberty to stimulatedevelopment of sex

    characteristics.

    Specialeducation to treat verbal

    ability problems.

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    Tuner syndrome (XO)- missingx chromosome. Short stature,

    webbed neck, incompletedevelopment of sex characteristicsat puberty, sterility and impairedspatial intelligence.

    1 in 2500 to 8000 female births.

    Hormone therapy in childhood tostimulate physical growth and atpuberty to promote development

    of sex characteristics. Special eduto treat spatial ability problems.

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    References