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Published byMerry Lambert Modified over 9 years ago
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Genetic Change G.Burgess 2012
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Chromosomal Dissorders Nondisjunction Deletion Duplication Translocation Inversion Genetic Dissorders Point mutation Insertion Deletion Splice site mutation Nonsense mutation Silent mutation Missense mutation
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Non Disjunction –Chromosomes do not separate during anaphase (non-disjunction) Both chromosomes go to one cell during anaphase causing one cell to have too many chromaomes and the other not having enough. –Example; Down Synrdom: trisomy 21 Klinefelters Syndrom: XXY XYY males XXX females Turner Syndrom: XO females
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Deletion When a part of a chromosome is lost during cell division Example –Cri du Chat: occurs with a deletion of part of chromosome 5.
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Duplication if a DNA fragment joins the homologous chromosome and that region is repeated Example –Fragile X
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Translocation a fragment of a chromosome is moved ("trans-located") from one chromosome to another –joins a non-homologous chromosome. –nothing has been gained or lost but it places genes in a new environment. Example –Acute Myelogenous Leukemia
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Point Mutations Single base substitutions –may occur as a single nucleotide base is replaced by other base. Examples: –Cystic fibrosis –Cancer –Sickle cell anemia –Tay sachs disease –Colour blindness
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Insertion/ deletion Addition or subtraction of nucleotide base(s) from a chromosome Example –Huntington`s Disease.
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Information Links for Genetic Dissorders http://www.rarechromo.org/html/hom e.asp, UNIQUE, understanding rare chromosomal disordershttp://www.rarechromo.org/html/hom e.asp http://www.chromodisorder.org/CDO/, Chromosomal disorder outreach.http://www.chromodisorder.org/CDO/
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