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Table 1 Clinical features of 26 males with Kallmann syndrome

From: Clinical and inheritance profiles of Kallmann syndrome in Jordan

FAMILY No Age Anosmia/hyposmia Synkinesia Hearing Impairment Renal abnormalities Azoospermia cryptorchidism Micropenis
1 1 46 +/H - + - + + -
  2 14 + + + + + + -
  3 27 + + - + + + -
  4 20 + + - + + + -
  5 20 + + - + + + -
  6 19 + + - + + + -
  7 16 + + - + + + -
  8 14 + + - + NA + -
  9 9 + + - + NA + +
  10 6 + + - - NA - +
  11 4 + + - - NA + +
II 1 37 + - - - + + +
  2 24 + - ND* ND* ND* + +
  3 22 + - ND* ND* ND* - +
  4 20 + - ND* ND* ND* + +
III 1 14 + + - - NA - +
  2 10 + + - + NA - +
  3 8 + + - + NA - +
IV 1 6 + + - - NA + +
  2 5 + + - - NA + +
V 1 20 +/H - + - + - +
  2 19 +/H + + + + - +
VI 1 19 + - - + ND + -
VII 1 37 + - - - + + +
VIII 1 22 + - - + + + +
IX 1 20 + - - - oligospermia + +
  1. NA: not applicable.
  2. ND: not done.
  3. *: lost contact
  4. H: hyposmia