Child Mr. Denton Mrs. Denton The first two generations of the Smith family, show
ID: 214463 • Letter: C
Question
Child Mr. Denton Mrs. Denton The first two generations of the Smith family, shown below, are healthy, so they are surprised when Laura and her husband Aaron, and Dylan and his wife Iris, have children, that show symptoms of a genetic disorder. Karer Leslie, and Lance have a rare condition called DiGeorge syndrome. The children have small facial features and low, rotated ears. More serious symptoms are defects in the blood vessels leading from the heart, impaired immunity, and disturbed calcium metabolism Dylan and Iris consult a genetic counselor, Ms. Reese, who is concerned that their niece Karen has the same syndrome as Leslie and Lance. She learns that Iris has had several spontaneous abortions, as has her sister-in- law, Laura. Noting the combination of repeated birth defects and pregnancy losses, Ms. Reese suggests that Dylan and Laura and their siblings, children, and parents be karyotyped. The results, unfortunately confirm the genetic consoler's suspicions. Perry, Holly, Ariel, Sherri, and Shane have normal chromosomes. Laura, Dylan, Zach and Kim have a balanced reciprocal translocation between chromosomes 20 and 22. They have no symptoms, but are translocation carriers with the following chromosomes. 3 Ariel Laura Aaron Perry Brenda Dylan | 1% áy Karen Sherri Shane Leslie Lance Kim Translocation Normal 22 Translocation Excess 22 Normal 20 Excess 20 Deficient 22 Deficient 20 Based on the information given above, answer the following five questions: (refer to the reciprocal translocation in the ppts of chapter 6).Explanation / Answer
4.b. 4 types : two normal and two abnormal gametes with excess or deficient genetic material are made in a normal carrier translocation.
7. F. Two of the above
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