Transcript
Page 1: Chromosomal aberrations

CHROMOSOMAL

ABERRATIONS

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disruptions in the normal

chromosomal content of a cell and are a major cause of genetic

conditions in humans

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Cri du chat

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Deletion of part of the short arm of chromosome 5. "Cri du chat" means "cry of the cat" in French; the condition was so-named because affected babies make high-pitched cries that sound like those of a cat. Affected individuals have wide-set eyes, a small head and jaw, moderate to severe mental health issues, and are very short.

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DOWN SYNDROME

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Extra copy of chromosome 21 (trisomy 21). Characteristics include decreased muscle tone, stockier build, asymmetrical skull, slanting eyes and mild to moderate developmental disability

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Edward’s syndrome

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 extra presence of trisomy-18, the second-most-common trisomy. Symptoms include motor retardation, developmental disability and numerous congenital anomalies causing serious health problems. They have characteristic clenched hands and overlapping fingers.

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Jacobsen syndrome

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 terminal 11q deletion disorder. Those affected have normal intelligence or mild developmental disability, with poor expressive language skills. 

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Klinefelter’s syndrome

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usually sterile, and tend to be taller and have longer arms and legs than their peers. Boys with the syndrome are often shy and quiet, and have a higher incidence of speech delay and dyslexia.

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Patau syndrome

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Triple x syndrome

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XXX girls tend to be tall and thin and

have a higher incidence of dyslexia

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XYY SYNDROME

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Females with Turner syndrome often have a short stature, low hairline, abnormal eye features and bone development and a "caved-in" appearance to the chest

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