Discussion
Match the syndromes listed in Column I with the cause/symptoms listed in Column II
| Column I | Column II |
|---|---|
| P. Prader-Willi syndrome | (i) a collection of signs and symptoms due to prolonged exposure to corticosteroids like cortisol |
| Q. Down syndrome | (ii) a syndrome of inadequate reabsorption in the proximal renal tubule of the kidney |
| R. Cushing syndrome | (iii) a genetic disorder usually caused by the deletion of a part of chromosome 15 |
| S. Turner syndrome | (iv) a genetic disorder caused by the presence of all or part of a third copy of chromosome 21 |
| T. Fanconi syndrome | (v) a genetic condition in which a female has partially or completely missing an X chromosome |
Answer: C
The match is P-(iii); Q-(iv); R-(i); S-(v); T-(ii).
- Prader-Willi syndrome is usually caused by loss of the paternal copy of a region of chromosome 15 (15q11-q13).
- Down syndrome is caused by a third copy of all or part of chromosome 21.
- Cushing syndrome results from prolonged exposure to high levels of corticosteroids such as cortisol.
- Turner syndrome is a female with one X chromosome partly or wholly missing (45,X).
- Fanconi syndrome is a failure of reabsorption in the proximal renal tubule.
The other options swap the chromosomal disorders or attach the kidney or steroid descriptions to genetic syndromes.
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