A 5-year-old boy with mental retardation is grossly obese and has facial features of Prader-Willi syndrome (PWS). Karyotyping and fluorescent in situ hybridization studies do not show deletion in the usual site on chromosome 15. Which of the following findings is most likely to confirm PWS in this child? A Deletion in the short arm of chromosome 15 BY Duplication within chromosome 15 Large trinucleotide repeat expansion in the PWS area of chromosome 15 (D)Maternal origin of both chromosomes 15 Translocation in the short arm of chromosome 15

Human Anatomy & Physiology (11th Edition)
11th Edition
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Chapter1: The Human Body: An Orientation
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A 5-year-old boy with mental retardation is grossly obese and has facial features of Prader-Willi syndrome (PWS). Karyotyping and fluorescent in situ hybridization studies do not
show deletion in the usual site on chromosome 15. Which of the following findings is most likely to confirm PWS in this child?
✓
A Deletion in the short arm of chromosome 15
BY Duplication within chromosome 15
Large trinucleotide repeat expansion in the PWS area of chromosome 15
D) Maternal origin of both chromosomes 15
-Translocation in the short arm of chromosome 15
Transcribed Image Text:A 5-year-old boy with mental retardation is grossly obese and has facial features of Prader-Willi syndrome (PWS). Karyotyping and fluorescent in situ hybridization studies do not show deletion in the usual site on chromosome 15. Which of the following findings is most likely to confirm PWS in this child? ✓ A Deletion in the short arm of chromosome 15 BY Duplication within chromosome 15 Large trinucleotide repeat expansion in the PWS area of chromosome 15 D) Maternal origin of both chromosomes 15 -Translocation in the short arm of chromosome 15
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