Questions
Multiple fill-in-the-blank
Question at position 18 Match the syndrome to the cause.Prompt 1cri du chatAnswer for prompt 1 cri du chat[input]Prompt 2Triple X syndromeAnswer for prompt 2 Triple X syndrome[input]Prompt 3Down syndromeAnswer for prompt 3 Down syndrome[input]Prompt 4Turner syndromeAnswer for prompt 4 Turner syndrome[input]Prompt 5Klinefelter syndromeAnswer for prompt 5 Klinefelter syndrome[input]Possible answerstrisomy 21deletion on chromosome 5X0XXXXXY
Options
A.trisomy 21
B.deletion on chromosome 5
C.X0
D.XXX
E.XXY
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Step-by-Step Analysis
Here is how each option maps to the prompts and why each choice is correct or not for that prompt.
Prompt 1 (cri du chat): The characteristic chromosomal alteration associated with cri du chat is a deletion on chromosome 5. Among the options, 'deletion on chromosome 5' is the correct match for cri du chat, because the syndrome results from a partial deletion of the short arm of chromosome 5 (5p-).
Option: trisomy 21 — this describes Down syndrome, not cri du chat, so it is incorrect for prompt 1.
Option: deletion on chromosome 5 — this is the acc......Login to view full explanationLog in for full answers
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