Try it
ENT · Nose: Kallmann syndrome
Sample itemA 17-year-old boy has absent puberty and has never perceived smell. Which hormonal finding is expected?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
B. Low GnRH-dependent gonadotropins (hypogonadotropic hypogonadism)
Kallmann syndrome results from failure of GnRH neurons to migrate with the olfactory placode, causing hypogonadotropic hypogonadism and anosmia. MRI shows absent olfactory bulbs. Treatment is hormone replacement.
Option by option
A. Low TSH
TSH is not related.
B. Low GnRH-dependent gonadotropins (hypogonadotropic hypogonadism) (correct)
Correct. Low gonadotropins with anosmia define Kallmann syndrome.
C. High FSH and LH
High FSH and LH would indicate primary gonadal failure.
D. High prolactin
Hyperprolactinaemia is not the mechanism.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
More ENT questions
- AudiologyIn a tuning fork test, Rinne is negative (bone conduction louder than air conduction) in…
- EarWhich type of chronic suppurative otitis media is considered 'unsafe'?
- LarynxIn singers, vocal nodules typically occur at:
- Vestibular disordersA patient has recurrent attacks of vertigo lasting hours, with fluctuating low-frequency…