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Karyotyping
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Karyotyping Techniques:
1) Chorionic Villus Sampling (CVS) – performed at 8 to 10 weeks gestation. 2) Amniocentesis – performed at 14 to 16 weeks gestation
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Some disorders checked for by amniocentesis are:
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Ultrasound
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Amniocentesis
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Process used to grow the baby’s cells
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Chromosomes are arranged in size order # 1 to 22 followed by the sex chromosomes(#23)
Karyotype 1
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Description of Karyotype 1
Gender: Female # of Chromosomes: 46 Disorder: No
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Karyotype 2 Three chromosomes at one spot (instead of 2) is called TRISOMY. This karyotype is showing TRISOMY 21 aka Down’s Syndrome
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Description of Karyotype 2
Gender: Female # of Chromosomes: 47 Disorder: Trisomy 21 a.k.a. Down’s Syndrome Unfortunately, it’s the most common trisomy disorder.
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What is Down’s Syndrome?
Down syndrome some degree of mental retardation characteristic facial features. Sometimes have congenital heart defects Many have some visual and hearing impairment. The severity varies greatly.
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Karyotype 3
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Description of Karyotype 3
Gender: Male # of Chromosomes: 47 Disorder: Trisomy 18 a.k.a. Edward’s syndrome Rick Santorum (republican candidate) and his daughter, Isabella, who has Trisomy 18
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What is Edward’s Syndrome?
Trisomy 18 is usually fatal*, with most of the babies dying before birth and those who do make it to birth typically living only a few days. However, a small number of babies (<10%) live at least one year. * characteristics include: a hole between the upper and/or lower chambers of the heart, a narrowing of the exit vessel from the heart, kidney abnormalities, a portion of the intestinal tract can be located outside the stomach in a sac, the esophagus does not connect to the stomach, meaning the baby cannot eat by mouth, clenched hands, rocker bottom feet, small jaw, and developmental delays.
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Karyotype 4
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Description of Karyotype 4
Gender: Female # of Chromosomes: 45 Disorder: Turner’s Syndrome (only 1 X)
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Turner’s Syndrome Absent or incomplete development at puberty, including sparse pubic hair and small breasts Broad, flat chest shaped like a shield Drooping eyelids and dry eyes Possible Infertility No periods (absent menstruation) Short height
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Karyotype 5
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Description of Karyotype 5
Gender: male # of Chromosomes: 47 Disorder: Klinefelter’s Syndrome
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Klinefelter’s low levels of the hormone testosterone beginning during puberty. Possible breast development (gynecomastia), reduced facial and body hair Possible infertility Female fat distribution (wide hips)
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Photo of Klinefelter’s Syndrome
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Karyotype 6
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Karyotype 6 Gender: Female # of Chromosomes: 47 Disorder: yes
Trisomy 13: Patau Syndrome
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Trisomy 13: Patau Syndrome
Polydactyl Cleft palate Mental retardation 90 -95% die within the first year
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Hermaphrodite Genetically XX XY 48 Chromosomes
Has both female and male genitalia. extremely rare
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