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Karyotypes& Chromosome Mutations
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A karyotype is an organized profile of a person's chromosomes
A normal human karyotype has 46 chromosomes (23 pairs): #1-22 are called autosomes #23 are called sex chromosomes
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XX~ female XY~ male
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Chromosomal Mutations
Change in # of chromosomes OR structure of the chromosome Mutations can only be inherited if they occur in sex cells
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Can YOU spot the chromosomal mutation??
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1) Deletion Loss of all or part of a chromosome
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2) Duplication Produce extra copies of parts of a chromosome.
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3) Inversion Part of a chromosome breaks out and reinserts backwards.
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4) Translocation Part of a chromosome breaks off & attaches to another chromosome
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5) Nondisjunction Improper separation of homologous chromosomes during meiosis Results in extra or missing chromosomes in gametes
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Remember—normally have 2 copies of each
Types of Nondisjunction Trisomy~ 3 copies of a chromosome Monosomy~ 1 copy of a chromosome Remember—normally have 2 copies of each
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Can you spot the mutation?
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Down Syndrome – Trisomy 21
Intellectual and developmental disabilities may have heart defects and respiratory problems
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Look at the karyotype for the mutation
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Trisomy on Sex Chromosomes
XYY Syndrome – Extra Y XXX Syndrome – Triple X
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What is the mutation? Boy or Girl?
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Trisomy 13 (Patau syndrome)
Extra fingers or toes Cleft lip or palate (deformed lips) Heart and brain structure problems Die within 1-2 years of age
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What is the mutation? Boy or Girl?
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Turner’s Syndrome 45,X Webbed neck Infertile
Swollen hands & feet at birth Heart defects
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